http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5037992-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C303-24
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-02
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C305-14
filingDate 1989-12-18^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1991-08-06^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_78a1da5105a6cb8487f12ca63ab77f43
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3a057dccdfbaed1868d0e89836fad36d
publicationDate 1991-08-06^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5037992-A
titleOfInvention Process for sulfating unsaturated alcohols
abstract The present invention is directed to a process for sulfating unsaturated alcohols using inexpensive reagents and mild reaction conditions. The process comprises reacting an unsaturated alcohol of the formula R--OH, wherein R is a C 8 -C 22 alkenyl group, with an ether sulfate of the formula R 1 (OCH 2 CH 2 ) n OSO 3 M, wherein R 1 is a C 1 -C 18 hydrocarbyl group, n is an integer from 1 to 10, and M is an alkali metal, to form an unsaturated sulfate; said reaction being carried out in the presence of a catlaytically effective amount of an acid catalyst. The mole ratio of unsaturated alcohol reactant to ether sulfate ranges from about 0.5:1 to about 2:1. In this process the sulfation occurs primarily at the hydroxyl group of the unsaturated alcohol, with minimal sulfation at the olefinic moiety of said alcohol.
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7861
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128880496
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID15066111
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID936
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID14250
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID87068530
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