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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1682741Generated: November 2, 2026

Sodium borohydride → 2(S)-t-Butyldimethylsilyloxy-2-phenylethanol

https://huagongshe.com/reaction/1682741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactantethyl (S)-alpha-(t-butyldimethylsilyloxy)-alpha-phenylacetateHCID 10968419—
SolventMethanolHCID 887—
Product2(S)-t-Butyldimethylsilyloxy-2-phenylethanolHCID 22867081—

Reaction Steps

15.5 g of sodium borohydride were added in portions, whilst ice-cooling, to a solution of 20 g of ethyl (S)-α-t-butyldimethylsilyloxy-α-phenylacetate [prepared as described in step (a) above] in 500 ml of absolute methanol, and the resulting mixture was stirred overnight at room temperature. At the end of this time, 10 g of sodium borohydride were added in portions, whilst ice-cooling. The reaction mixture was then stirred at room temperature for 5 hours, after which it was concentrated by evaporation under reduced pressure, and the concentrate was mixed with water and ethyl acetate. The ethyl acetate layer was separated, washed with water and dried over anhydrous sodium sulfate, and then the solvent was removed by distillation under reduced pressure, to give the title compound as a crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05635534
Source datasetuspto-grants-1997_06
ORD IDord-a5b7f5b8d1db4817a34e55de5a6fbaa2
Source noteuspto-grants-1997_06