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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026562Generated: November 1, 2026

Dichloromethane → (2S)-4-{[tert-butyl(diphenyl)silyl]oxy}butan-2-ol

https://huagongshe.com/reaction/1026562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantAmmonium ChlorideHCID 25517—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
Reactant(+)-1,3-ButanediolHCID 446973—
SolventTriethylamineHCID 8471—
Product(2S)-4-{[tert-butyl(diphenyl)silyl]oxy}butan-2-olHCID 58005224—

Reaction Steps

Under ice cooling, to a dichloromethane solution (20.0 ml) of (S)-1,3-butanediol (519 mg) were added triethylamine (1.04 ml) and tert-butylchlorodiphenylsilane (1.63 ml), followed by stirring at room temperature overnight. The reaction solution was poured into a saturated aqueous ammonium chloride solution, and extracted with ethyl acetate. The organic layer was washed with saturated sodium chloride solution, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The resulting residue was purified by silica gel chromatography to afford (2S)-4-{[tert-butyl(diphenyl)silyl]oxy}butan-2-ol (1.69 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729095B2
Source datasetuspto-grants-2014_05
ORD IDord-25728101a12f47a6b6ac19b9099b809e
Source noteuspto-grants-2014_05