HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1901198Generated: November 1, 2026
Sodium borohydride → 2(S)-t-Butyldimethylsilyloxy-2-phenylethanol
https://huagongshe.com/reaction/1901198
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | ethyl (S)-alpha-(t-butyldimethylsilyloxy)-alpha-phenylacetate | HCID 10968419 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2(S)-t-Butyldimethylsilyloxy-2-phenylethanol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05576340 |
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| Source dataset | uspto-grants-1996_11 |
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| ORD ID | ord-240dca1db7e84c01aadd378b11569c36 |
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| Source note | uspto-grants-1996_11 |
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