Hydrochloric Acid → HCID 178444473, compound

A solution of 13.5 g of ethyl (E)-3-(trans-4-pentylcyclohexyl)acrylate in 100 ml of dichloromethane was treated dropwise at -78° C. and while gassing with nitrogen with a 20% solution of diisobutylaluminium hydride in hexane. After completion of the addition the slightly yellow solution was stirred for a further 1 hour and then treated cautiously with 10 ml of 25% hydrochloric acid. The reaction mixture was poured into 100 ml of water and the organic phase was separated. The aqueous phase was back-extracted twice with 100 ml of dichloromethane each time. The combined organic phases were washed with 500 ml of water, 500 ml of concentrated potassium hydrogen carbonate solution and again with 500 ml of water and subsequently dried over magnesium sulphate, filtered and concentrated. Distillation of the residue gave 10 g of (E)-3-(trans-4-pentylcyclohexyl)allyl alcohol with b.p. 174°-175° C./15 mmHg.

1. additionAfter completion of the addition the slightly yellow solution
2. customthe organic phase was separated
3. extractionThe aqueous phase was back-extracted twice with 100 ml of dichloromethane each time
4. washThe combined organic phases were washed with 500 ml of water, 500 ml of concentrated potassium hydrogen carbonate solution and again with 500 ml of water
5. dry with materialsubsequently dried over magnesium sulphate
6. filtrationfiltered
7. concentrationconcentrated
8. distillationDistillation of the residue

ORD record

ord-802dd918c9e44fee851540eea87b19a5

Source dataset

uspto-grants-1995_05

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05411676