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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734908Generated: November 1, 2026

Ethanol → HCID 54480844, compound

https://huagongshe.com/reaction/1734908

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantHCID 19966152HCID 19966152—
ReactantHCID 67706647HCID 67706647—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
ProductHCID 54480844HCID 5448084498%

Reaction Steps

A solution of 3.46 g (9.55 mmol) of (S)-[3-benzyloxy-2-(t-butyldimethylsilyloxypropyl)cyclohexane [prepared as described in step (ii) above] in 50 ml of ethanol was vigorously stirred for 5 hours and 20 minutes in a stream of hydrogen and in the presence of 580 mg of 10% w/w palladium-on-charcoal. At the end of this time, the reaction mixture was filtered, and the catalyst was washed with ethanol. The filtrate and the washings were combined and the solvent was removed by distillation under reduced pressure. The resulting residue was purified by column chromatography through 180 g of silica gel, using a 1:4 by volume mixture of ethyl acetate and hexane as the eluent, to give 2.54 g (yield 98%) of the title alcohol derivative as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05534529
Source datasetuspto-grants-1996_07
ORD IDord-7cfe5cb5f41c470289f08d857d3473c9
Source noteuspto-grants-1996_07