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filingDate 1970-04-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1971-11-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1897dfc9570e601bca833732321ed7a5
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publicationDate 1971-11-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-3624106-A
titleOfInvention Tetrahydropyranyl ether of 3-endo-methyl-3-exo(4{40 -methyl-5{40 -hydroxypentyl) norcamphor
abstract The novel compounds, 2-methyl-5-bromopentyl tetrahydropyranyl ether and tetrahydropyranyl ether of 3-endo-methyl-3-exo(4''methyl-5''-hydroxypentyl)norcamphor and a process for preparing 2methyl-5-bromopentyl tetrahydropyranyl ether, tetrahydropyranyl ether of 3-endo-methyl-3-exo(4''-methyl-5''hydroxypentyl)norcamphor and 3-endo-methyl-3-exo(4''-methyl-5''hydroxypentyl)norcamphor comprising the steps of: (1) esterifying 2-methyl-4-pentenol; (2) hydrobrominating the ester in the presence of a free radical catalyst; (3) reducing the hydrobrominated ester to 2-methyl-5-bromopentanol; (4) etherifying 2-methyl-5-bromopentanol with dihydropyran to obtain the novel compound, 2-methyl-5-bromopentyl tetrahydropyranyl ether; (5) alkylating 3-methylnorcamphor with the 2-methyl-5bromopentyl tetrahydropyranyl ether to obtain the novel compound, tetrahydropyranyl ether of 3-endo-methyl-3-exo(4''-methyl-5''hydroxypentyl)norcamphor; and (6) treating tetrahydropyranyl ether of 3-endo-methyl-3-exo(4''-methyl-5''hydroxypentyl)norcamphor with p-toluenesulfonic acid or hydrochloric acid to obtain 3-endo-methyl-3-exo(4''-methyl-5''hydroxypentyl)norcamphor.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9900377-A1
priorityDate 1970-04-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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