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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C01B35-061
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C01B35-06
filingDate 1979-03-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1980-07-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_62d44adc28f0845023d713d821d6dee7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e259ec9e7987f58d9973a495be9bb8c0
publicationDate 1980-07-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4210631-A
titleOfInvention Preparation of boron trichloride
abstract Boron trichloride is prepared in substantially stoichiometric quantities by free-radical chlorination of borate ester, e.g., trimethyl borate, at temperatures of between about 20° C. and 100° C., more preferably between about 40° C. and about 90° C. The mole ratio of chlorine to borate ester is from about 5.5:1 to about 7.5:1. Reactor pressures are moderate, e.g., generally less than 3 atmospheres absolute. Atmospheric pressure can be used. An inert liquid organic solvent, e.g., carbon tetrachloride, can be used as the reaction medium. Gaseous reaction products are removed from the reactor during the chlorination reaction. In addition to boron trichloride, carbon monoxide (rather than phosgene) and hydrogen chloride are the principal products of the chlorination reaction. Phosgene is produced in substantially lower amounts than when chlorination is conducted at autogeneous pressures and the chlorine:trimethyl borate mole ratio is 9:1 or more. The boron trichloride product is separated from the carbon monoxide, hydrogen chloride and phosgene products, and recovered.
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