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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35790Generated: October 29, 2026

Hydrochloric Acid → HCID 178444473, compound

https://huagongshe.com/reaction/35790

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantDiisobutylaluminumhydrideHCID 21225700—
ReactantHCID 178444478HCID 178444478—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
ProductHCID 178444473HCID 17844447388.9%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05411676
Source datasetuspto-grants-1995_05
ORD IDord-802dd918c9e44fee851540eea87b19a5
Source noteuspto-grants-1995_05