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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372612Generated: November 1, 2026

alpha-Cyclocitral → 2,6,6-Trimethylcyclohex-2-ene-1-methanol

https://huagongshe.com/reaction/372612

Reaction equation

Participants

RoleNameHCIDCharge
Reactantalpha-CyclocitralHCID 94143—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
Product2,6,6-Trimethylcyclohex-2-ene-1-methanolHCID 9793271.1%

Reaction Steps

To a suspension of 1.25 g NaBH4 in 50 ml. 95% ethanol cooled in an ice bath was added dropwise with stirring 5.0 g alpha-cyclocitral which had been prepared as described in Example 1. When the addition was complete, the ice bath was removed and water was added to dissolve any remaining solids. The reaction mixture was then stirred overnight at room temperature. The solvent was removed at reduced pressure and the residue taken up in ether, washed with 1 N acetic acid, dilute sodium bicarbonate and water. The ether extract was dried over sodium sulfate and concentrated to give 3.6 g alpha-cyclogeraniol as a colorless oil of 95% purity by gas chromatographic analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04091823
Source datasetuspto-grants-1978_05
ORD IDord-d8f23aa72d334b6e9e4242040fde1b20
Source noteuspto-grants-1978_05