http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1000763-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_445a797690bdb3709f7c1a0a64853ba2
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08K5-375
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C323-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08K5-375
filingDate 1961-05-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_71e12a3e890740b1e36d4371353bbaaf
publicationDate 1965-08-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1000763-A
titleOfInvention Preparation of substituted phenols
abstract Alkylmercaptophenols or alkylmercaptophenol ethers are produced by reacting a phenol or a phenol ether with an alkyl sulphenyl halide which is formed in the reaction mixture by reacting an alkyl disulphide or alkyl mercaptan with a halogen. The alkyl sulphenyl halide may contain 1-18, preferably 1-12, carbon atoms in the alkyl group. The reaction is preferably effected under anhydrous conditions with or without a solvent, e.g. carbon tetrachloride. An excess of phenol or phenol ether is preferably used. In a typical example, (I) p-hydroxyphenylmethyl sulphide is obtained by chlorinating a mixture of dimethyl disulphide and phenol in carbon tetrachloride at - 10 DEG to - 20 DEG C. Other examples describe the preparation of p-hydroxyphenyl butyl sulphide, p-hydroxyphenyl n-dodecyl sulphide, p - hydroxyphenyl - tert. - butyl sulphide and 2-hydroxynaphthyl-1 butyl sulphide. 1-Chloro-2-naphthol is obtained as a by-product in the preparation of 2-hydroxynaphthyl-1 butyl sulphide. Anisol is another specified phenol which may be treated. Reference has been directed by the Comptroller to Specification 875,464.
priorityDate 1961-05-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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