HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828807Generated: November 1, 2026
Sodium borohydride → HCID 69527632, compound
https://huagongshe.com/reaction/1828807
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 22058586 | HCID 22058586 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 69527632 | HCID 69527632 | 94.6% |
Reaction Steps
To a suspension of 4-((tert-butyldiphenylsiloxy)methyl)-3-chlorobenzaldehyde (3.24 g) in ethanol (32 ml) was added sodium borohydride (149 mg) under ice-cooling and the mixture was stirred at room temperature for 3 hr. The reaction mixture was concentrated to about half amount. Water was added and the resulting product was extracted twice with diisopropyl ether. The organic layers were combined, washed successively with saturated aqueous sodium hydrogencarbonate solution and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated and the residue was purified by silica gel column chromatography (hexane/ethyl acetate=5/1) to give 4-((tert-butyldiphenylsiloxy)methyl)-3-chlorobenzyl alcohol (3.08 g) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07060721B1 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-27354e00d3b34f24ae97da49e0cbe085 |
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| Source note | uspto-grants-2006_06 |
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