Patent classifications
C07D307/46
Production of purified dialkyl-furan-2,5-dicarboxylate (DAFD) in a retrofitted DMT plant
Disclosed is a process to produce a purified vapor comprising dialkyl-furan-2,5-dicarboxylate (DAFD). Furan-2,5-dicarboxylic acid (FDCA) and an alcohol in an esterification zone to generate a crude diester stream containing dialkyl furan dicarboxylate (DAFD), unreacted alcohol, 5-(alkoxycarbonyl)furan-2-carboxylic acid (ACFC), and alkyl furan-2-carboxylate (AFC). The esterification zone comprises at least one reactor that has been previously used in an DMT process.
Production of purified dialkyl-furan-2,5-dicarboxylate (DAFD) in a retrofitted DMT plant
Disclosed is a process to produce a purified vapor comprising dialkyl-furan-2,5-dicarboxylate (DAFD). Furan-2,5-dicarboxylic acid (FDCA) and an alcohol in an esterification zone to generate a crude diester stream containing dialkyl furan dicarboxylate (DAFD), unreacted alcohol, 5-(alkoxycarbonyl)furan-2-carboxylic acid (ACFC), and alkyl furan-2-carboxylate (AFC). The esterification zone comprises at least one reactor that has been previously used in an DMT process.
SYNTHESIS OF OLEOFURANS
Disclosed herein is a method for making oleofuran compounds according to formula 3
##STR00001##
from a furan aldehyde or ketone and a fatty alcohol. The method comprises combining the furan compound and the fatty acid in the presence of a first catalyst to form an intermediate compound, and exposing the intermediate compound to hydrogen in the presence of a second catalyst to form the oleofuran compound. The hydrogen may be either hydrogen gas or hydrogen provided by a hydrogen donor.
SYNTHESIS OF OLEOFURANS
Disclosed herein is a method for making oleofuran compounds according to formula 3
##STR00001##
from a furan aldehyde or ketone and a fatty alcohol. The method comprises combining the furan compound and the fatty acid in the presence of a first catalyst to form an intermediate compound, and exposing the intermediate compound to hydrogen in the presence of a second catalyst to form the oleofuran compound. The hydrogen may be either hydrogen gas or hydrogen provided by a hydrogen donor.
COMPOUNDS AND METHODS FOR HEMATOPOIETIC REGENERATION
The invention relates to compounds that promote hematopoietic regeneration. The invention further relates to methods of promoting hematopoietic regeneration using the novel compounds of the invention.
Complexes
The present invention provides a palladium(II) complex of formula (1).
##STR00001##
R.sub.12, m, and X are described in the specification.
The invention also provides a process for the preparation of the complex, and its use in carbon-carbon and carbon-heteroatom coupling reactions.
Complexes
The present invention provides a palladium(II) complex of formula (1).
##STR00001##
R.sub.12, m, and X are described in the specification.
The invention also provides a process for the preparation of the complex, and its use in carbon-carbon and carbon-heteroatom coupling reactions.
A SINGLE STEP PROCESS FOR THE SYNTHESIS OF FURAN DERIVATIVES FROM CARBOHYDRATES
The present invention discloses a single step process for the synthesis of furan derivative from carbohydrate comprises stirring the reaction mixture of carbohydrate in solvent in presence of catalyst at temperature in the range of 170 to 190° C. for the period in the range of 23 to 25 hrs to afford corresponding furan derivative.
A SINGLE STEP PROCESS FOR THE SYNTHESIS OF FURAN DERIVATIVES FROM CARBOHYDRATES
The present invention discloses a single step process for the synthesis of furan derivative from carbohydrate comprises stirring the reaction mixture of carbohydrate in solvent in presence of catalyst at temperature in the range of 170 to 190° C. for the period in the range of 23 to 25 hrs to afford corresponding furan derivative.
Syntheses of allyl phosphine complexes of palladium
The present invention provides a palladium(II) complex of formula (1) or a palladium(II) complex of formula (2). ##STR00001## R.sub.1, R.sub.2, R.sub.3, R.sub.4, R.sub.5, R.sub.6, R.sub.7, R.sub.8, R.sub.9, R.sub.10, R.sub.11, R.sub.12, R.sub.18, R.sub.19, R.sub.20, R.sub.21, R.sub.22, R.sub.23 and R.sub.24, m, E and X are described in the specification. The invention also provides a process for the preparation of the complexes, and their use in carbon-carbon and carbon-heteroatom coupling reactions.