METHOD FOR THE PHOSGENATION OF COMPOUNDS COMPRISING HYDROXYL, THIOL, AMINO AND/OR FORMAMIDE GROUPS

Abstract

A method of reacting a first compound with a second compound, wherein the first compound has a GHS hazard identification of GHS06 and is obtainable from the reaction of at least one first fluid precursor compound and one second fluid precursor compound and wherein the second compound is capable of a chemical reaction with the first compound is provided

Claims

1. A method of reacting a first compound with a second compound, wherein the first compound has a GHS hazard identification of GHS06 and is obtainable from the reaction of at least one first fluid precursor compound and one second fluid precursor compound and wherein the second compound is capable of a chemical reaction with the first compound, comprising: (I) providing a liquid phase containing the second compound in a reactor having an upper end and a lower end viewed in the direction of gravity; (II) providing a contact tube having an upper end and a lower end in the reactor, wherein the lower end of the contact tube is immersed into the liquid phase containing the second compound and a catalyst bed present in the contact tube is set up to catalyze the reaction between the first and second precursor compounds to give the first compound; (III) introducing the first and second precursor compounds through the contact tube, with the first compound formed in the contact tube exiting from the lower end of the contact tube and coming into contact with liquid phase containing the second compound.

2. The method as claimed in claim 1, wherein the first compound is phosgene, the first precursor compound is carbon monoxide, the second precursor compound is chlorine, the catalyst present in the catalyst bed is an activated carbon catalyst and the second compound is a compound containing one or more of hydroxyl, thiol, amino and/or formamide groups.

3. The method as claimed in claim 2, wherein the activated carbon catalyst has a BET surface area of ≧300 to ≦2000 m.sup.2/g and a d.sub.90 of the particle size distribution of 25 μm to 4 mm.

4. The method according to claim 1, wherein the method is conducted in a reactor comprising: a hood at the upper end of the reactor, bounded by a tube plate within the reactor; a multitude of contact tubes arranged in longitudinal direction of the reactor, the contact tubes being secured on the tube plate by upper ends thereof; and wherein the liquid phase containing the second compound is provided in an interspace around the contact tubes.

5. The method as claimed in claim 1, wherein a catalyst is additionally present in the liquid phase containing the second compound.

6. The method as claimed in claim 1, wherein the contact tube(s) has/have a ratio of length to diameter of ≧15:1 to ≦1600:1.

7. The method as claimed in claim 1, wherein the sum total of the partial pressures of the first precursor compound and the second precursor compound is ≧1 bar to ≦26 bar.

8. A reactor for reaction of phosgene with one or more compounds containing one or more hydroxyl, thiol, amino and/or formamide groups, comprising: a hood at the upper end of the reactor, bounded by a tube plate within the reactor; a multitude of contact tubes arranged in longitudinal direction of the reactor, the contact tubes being secured on the tube plate by upper ends thereof, wherein a catalyst bed present in the contact tubes is set up to catalyze the reaction of carbon monoxide and chlorine; the reactor is set up to introduce carbon monoxide and chlorine gas into space formed between the hood and tube plate, such that these gases flow through the contact tubes; the reactor is set up to introduce a compound containing one or more hydroxyl, thiol, amino and/or formamide groups into an interspace around the contact tubes and to withdraw one or more liquid reaction products of said compound with phosgene from said interspace and the reactor is additionally set up to withdraw one or more gaseous reaction products on a side of the tube plate facing away from the hood.

9. The reactor as claimed in claim 8, wherein activated carbon catalyst utilized therein has a BET surface area of ≧300 to ≦2000 m.sup.2/g and a d.sub.90 of the particle size distribution of 25 μm to 4 mm.

10. The reactor as claimed in claim 8, wherein the contact tubes have a ratio of length to diameter of ≧15:1 to ≦1600:1.

Description

[0054] The present invention is elucidated in detail by the figures and examples which follow, but without being limited thereto. The figures show:

[0055] FIG. 1 a cross section through a reactor for the method of the invention

[0056] FIG. 2 a cross section through a reactor of the invention

[0057] FIG. 1 shows a schematic cross section through a reactor in which the method of the invention is conducted. A stirred tank reactor with a lateral heating/cooling jacket was charged with molten phenol. The height of the liquid level is illustrated by the dotted line in the reactor. A contact tube 100 with an activated carbon fixed catalyst bed is arranged within the reactor, with the lower end of the contact tube 100 immersed into the molten phenol.

[0058] Via the conduit 101, gas introduced into the reactor can be removed again. The gas may, for example, be nitrogen when the reactor is inertized prior to commencement of the reaction. In addition, substances can be introduced into the reactor via the conduit 101. These may especially be catalysts for the preparation of DPC, for example TiCl.sub.4.

[0059] The temperature sensor TX1 measures the temperature in the liquid phase within the reactor. The temperature within the contact tube is measured by the temperature sensor TX2.

[0060] As carbon monoxide and chlorine pass through the contact tube 100, phosgene is formed, which exits from the lower end of the contact tube 100 in the form of gas bubbles and rises upward through the phenol. In the course of this, DPC is formed.

[0061] FIG. 2 shows a schematic cross section through a reactor of the invention in which the method of the invention is conducted. At its upper end, viewed in relation to the direction of gravity, is a hood 200. Also present within the reactor is a tube plate 300 which bounds the hood 200 in the interior. This forms a gas space 500.

[0062] The tube plate 300 bears a plurality of contact tubes 110 secured by their upper ends in the tube plate 300. The contact tubes 110 are arranged in longitudinal direction of the reactor. On the side remote from the tube plate 300, the contact tubes 110 form an interspace 400.

[0063] The interspace 400 is charged with liquid phenol. The height of the liquid level is illustrated by the dotted line in the reactor. Carbon monoxide and chlorine gas are introduced simultaneously into the hood 200, mix in the space 500 pass through the orifices into the contact tubes 110 at the upper end thereof. As already outlined above, phosgene is formed in the contact tubes 110, exits from the lower ends of the contact tubes 110 at the orifices, rises upward through the phenol and reacts with the phenol as it does so to form DPC.

[0064] At the upper end of the liquid level, DPC and excess phenol (“PhOH(exc.)”) are withdrawn. Above the liquid level, on the side of the tube plate 300 facing away from the hood 200, the gaseous HCl and excess carbon monoxide (“CO(exc.)”) components are withdrawn.

[0065] The tube plate 300 has no further orifices aside from the orifices which are formed by the upper ends of the contact tubes 110. In this way, the gas space 500 can be separated from the interspace 400. This has the advantage that contact of chlorine gas with phenol and the formation of chloroaromatics as by-products can be avoided.

EXAMPLES

Performance of the Method of the Invention on the Laboratory Scale

[0066] The experimental setup was analogous to the schematic arrangement shown in FIG. 1. A 600 mL pressure reactor equipped with a sparging stirrer and internal thermometer (cf. TX1 in FIG. 1) was charged with 280.4 g (2.98 mol) of phenol and the latter was melted by heating to about 45-50° C. The catalyst cartridge (cf. 100 in FIG. 1; length: 118 mm, diameter: 12 mm) was charged with 2.59 g of activated carbon powder (particle size 45-125 μm) and screwed to the lid of the pressure vessel in a gas-tight manner. The base of the cartridge was provided with a hole (diameter 0.5 mm). In a stream of nitrogen, the reactor lid provided with the integrated catalyst cartridge (cf. 100 in FIG. 1) was screwed on and hence the catalyst cartridge was immersed into the phenol melt. The internal cartridge temperature was measured by means of a further thermocouple (cf. TX2 in FIG. 2) in a central cartridge position. The reactor outlet (cf. conduit 101 in FIG. 1) was still open at this time and the reactor was inertized by the constant N.sub.2 stream (6.0 mL/min) while stirring for 30 min. Subsequently, through the valve present in this conduit (cf. conduit 101 in FIG. 1), 0.1 mL of TiCl.sub.4 was added to the liquid PhOH. The mixture was heated to 200° C. under a constant N.sub.2 flow (6.0 mL/min). The reactor outlet valve (cf. conduit 101 in FIG. 1) was closed here at an internal temperature of TX1=130° C. On attainment of internal reactor temperature 200° C., 4.5 mL/min of CO and 4.3 mL/min of Cl.sub.2 were metered in with simultaneous stoppage of the addition of N.sub.2 (catalyst cartridge; cf. 100 in FIG. 1). After introduction of a total of 1.12 L of CO (0.050 mol) and 1.06 L of Cl.sub.2 (0.047 mol), the addition of Cl.sub.2 and CO was ended and switched to 3.0 mL/min of N.sub.2. The pressure in the reactor at this time was 12 bar. The reaction mixture was stirred at 200° C. for 60 minutes and then cooled down to 50° C. over several hours. On attainment of 120° C., the reactor was decompressed. Under a still constant stream of N.sub.2 (3.0 mL/minute) and while stirring (2000 rpm), the reactor was inertized overnight and freed of possible residues of HCl, COCl.sub.2, CO or Cl.sub.2. The formation of DPC was detected by analysis of the product mixture obtained by means of gas chromatography.