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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648672Generated: October 29, 2026

Imidazole → (3S)-3-(tert-Butyldimethylsiloxy)-3-cyclohexylprop-1-yne

https://huagongshe.com/reaction/648672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
ReactantHexaneHCID 8058—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Product(3S)-3-(tert-Butyldimethylsiloxy)-3-cyclohexylprop-1-yneHCID 11983898—

Reaction Steps

To a solution of (S)-3-cyclohexylprop-1-yn-3-ol, (obtained according to Preparation 10) (2.76 g, 0.02 mol), in 10 ml N,N-dimethylformamide (DMF), cooled to 0° C., was added imidazole (2.1 g), followed by tert-butyldimethylchlorosilane (3.1 g, 0.02 mol). The mixture was stirred for 3 h. Water (80 ml) and hexane (80 ml) were added; the organic layer was separated and combined with 2×80 ml of hexane extractions of the aqueous layer. The solvent was removed (in vacuo), after drying over sodium sulfate, to give a crude residue (4.3 g) which was chromatographed on silica gel (80 g), eluting with ethyl acetate-hexane (2:1, v/v) to afford (S)-3-tert-butyldimethylsilyloxy-3-cyclohexylprop-1-yne.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04735966
Source datasetuspto-grants-1988_04
ORD IDord-cce85f4917e848c489e972ae28d5ec41
Source noteuspto-grants-1988_04