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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-52
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J27-125
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C2-68
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filingDate 1991-09-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f427feb4b36df41e63ef475012fe41ba
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0833fd53a737f01e39b38e6759862c1d
publicationDate 1993-04-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H0585958-A
titleOfInvention Method for producing 1,1,3,4,4,6-hexamethyltetralin
abstract (57) [Summary] [Objective] 1,1,3,4,4,6-hexamethyl from p-cymene, 3,3-dimethyl-1-butene and tertiary alkyl chloride in good yield and reproducibility. The purpose is to produce tetralin. Constitution: p-cymene, 3,3-dimethyl-1-butene and tertiary alkyl chloride are reacted in the presence of an anhydrous aluminum halide catalyst to give 1,1,3,4,4,6. -In a method for producing hexamethyltetralin, 2 Using the aliphatic hydrocarbon or chlorinated aliphatic hydrocarbon whose solubility coefficient at 5 ° C is 9.3 or less as a solvent, p- It is characterized by preliminarily charging 30 to 100% of cymen together with a solvent and reacting in the temperature range of 10 ° C to 30 ° C.
priorityDate 1991-09-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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