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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166421Generated: October 30, 2026

Benzyl Chloride → {(1R,6S)-6-[(Benzyloxy)methyl]cyclohex-3-en-1-yl}methanol

https://huagongshe.com/reaction/2166421

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantSodium hydrideHCID 24758—
Reactantcis-1,2-Dihydroxymethylcyclohex-4-eneHCID 11275057—
SolventDimethylformamideHCID 6228—
Product{(1R,6S)-6-[(Benzyloxy)methyl]cyclohex-3-en-1-yl}methanolHCID 6794654262.3%

Reaction Steps

The diol (1) (16.2 g) in dimethylformamide (50 ml) is added dropwise to sodium hydride (3.1 g) in dimethylformamide (DMF) (50 ml). The mixture is stirred for 20 minutes and then benzyl chloride (16 g) is added and stirring is continued for a further 18 hours at 70° C. After removing the DMF in vacuo, water is added and the mixture is extracted with ether. The combined extracts are dried (MgSO4) and the solvent is evaporated to give a residue which is distilled under reduced pressure to give the title compound as an oil (16.5 g, ca. 60%), b.p. 140°-145° C./0.03 mm, νmax (film) 3440 and 1600 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04945106
Source datasetuspto-grants-1990_07
ORD IDord-e40d7340a55643fab3198515ca37b132
Source noteuspto-grants-1990_07