C07B61/00

Method for producing 3-methylcycloalkenone compound
11377411 · 2022-07-05 · ·

The present invention relates to a method for producing a 3-methylcycloalkenone compound and a method for producing muscone. In the presence of a zirconium oxide catalyst, a diketone represented by the following general formula (1): ##STR00001##
wherein in formula (1), n represents 8, 9, 10, 11 or 12,
is subjected to a vapor-phase intramolecular condensation reaction, whereby a 3-methylcycloalkenone compound can be produced with high reaction efficiency. When a 3-methylcyclopentadecenone compound produced by this method is hydrogenated in a known manner, muscone can be produced efficiently.

METHOD FOR PRODUCING ALCOHOL
20220251009 · 2022-08-11 · ·

A method for producing an alcohol by hydrating an olefin using a heteropolyacid catalyst is provided, in which the catalyst can be stably used over a long period. The method is for producing an alcohol by supplying water and an olefin having 2-5 carbon atoms to a reactor and hydrating the olefin in a gas phase using a solid acid catalyst loaded with a heteropolyacid or a salt thereof, and is characterized in that a raw-material mixture to be supplied to the reactor has an aldehyde compound content of 70 mol ppm or less.

Catalyst and precursor thereof and method of forming dialkyl carbonate

A method of forming dialkyl carbonate is provided, which includes introducing carbon dioxide into a catalyst to form dialkyl carbonate, wherein the catalyst is formed by activating a catalyst precursor using alcohol, wherein alcohol is R.sup.3—OH, and R.sup.3 is C.sub.1-12 alkyl group or C.sub.5-12 aryl or heteroaryl group. The catalyst precursor is formed by reacting Sn(R.sub.1).sub.2(L).sub.2 and Ti(OR.sup.2).sub.4, and Sn(R.sup.1).sub.2(L).sub.2 and Ti(OR.sup.2).sub.4 have a molar ratio of 1:2 to 2:1. R.sup.1 is C.sub.1-10 alkyl group, R.sup.2 is H or C.sub.1-12 alkyl group, and L is O—(C═O)—R.sup.5, and R.sup.5 is C.sub.1-12 alkyl group. The dialkyl carbonate is ##STR00001##

METHOD FOR PRODUCING (METH)ACROLEIN AND METHOD FOR PRODUCING (METH)ACRYLIC ACID

A method for producing (meth)acrolein by vapor-phase catalytic oxidation of propylene or isobutylene in a multitubular reactor including a plurality of reaction tubes, the reaction tubes each including a reaction zone filled with a catalyst including molybdenum oxide and a cooling zone filled with an inert substance, wherein a temperature of a heat medium that flows outside the cooling zone is lower than a temperature of a heat medium that flows outside the reaction zone, and wherein the inert substance includes an inert substance having a major-axis length that is equal to or more than 1.7 times a major-axis length of the catalyst. A method for producing (meth)acrylic acid in which (meth)acrolein thus produced is converted to (meth)acrylic acid by vapor-phase catalytic oxidation.

METHOD FOR PRODUCING FLUOROPOLYETHER GROUP-CONTAINING COMPOUND

A method for producing a fluoropolyether group-containing compound, which includes reacting a fluoropolyether group-containing compound (A) represented by the formula (1) with a compound (C) represented by any of the formulae (c1) to (c4) in the presence of a metal catalyst including at least one selected from Pd, Cu, Ni, Pt, and Ag. The symboles are as defined herein.

##STR00001##

METHOD FOR PRODUCING FLUOROPOLYETHER-GROUP-CONTAINING COMPOUND

A method for producing a fluoropolyether group-containing compound, which includesreacting a fluoropolyether group-containing compound (A) represented by the following formula:


X.sup.11—(R.sup.11).sub.n11—R.sup.F1—X.sup.12  (1)

in the presence of a metal catalyst to form a fluoropolyether group-containing compound (B) containing two or more moieties derived from the fluoropolyether group-containing compound (A). Each of the above symbols is as defined in the description.

Polymer, Resist Composition, Method for Manufacturing Substrate Having Pattern Formed Therein, and (Meth)Acrylic Ester and Production Method Therefor

Provided is a polymer including a constituent unit (1) based on a monomer represented by Formula (1), in which a content of a constituent unit based on a monomer having a polycyclic structure is 35 mol % or less. In Formula (1), R.sup.1 represents a hydrogen atom or a methyl group, A.sup.1 represents a linking group including an ester bond, or a single bond, where A.sup.1 has no tertiary carbon atom, and Z.sup.1 represents an atomic group forming a sulfur-containing cyclic hydrocarbon group having 3 to 6 carbon atoms, which includes a carbon atom bonded to A.sup.1, and —SO.sub.2—.

##STR00001##

Method for Producing Herbicide Intermediate

A method for producing methyldichlorophosphane, the method including: allowing methane and phosphorus trichloride to react in the presence of an additive using a metal compound, or a metal compound carried on a carrier, or both thereof.

Method for Producing 1,1,1-Trifluoro-2,2-Bisarylethane, and 1,1,1-Trifluoro-2,2-Bisarylethane

The present invention has the effect of making it possible to produce 1,1,1-trifluoro-2,2-bisarylethane efficiently by a simple procedure by condensing a mixture of fluoral and hydrogen fluoride with an aryl compound under anhydrous conditions. The purity of the 1,1, 1-trifluoro-2, 2-bisarylethane obtained can be raised by a simple purification method such as crystallization or distillation. The obtained 1,1,1-trifluoro-2,2-bisarylethane can be increased in purity by a simple purification method such as crystallization operation or distillation.

Method for producing herbicide intermediate

A method for producing methyldichlorophosphane, the method including: allowing methane and phosphorus trichloride to react in the presence of an additive using a metal compound, or a metal compound carried on a carrier, or both thereof.