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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411253Generated: October 30, 2026

Imidazole → (S)-4-(tert-butyldimethylsilyloxy)butan-2-ol

https://huagongshe.com/reaction/411253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantDimethylformamideHCID 6228—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant(+)-1,3-ButanediolHCID 446973—
SolventDichloromethaneHCID 6344—
Product(S)-4-(tert-butyldimethylsilyloxy)butan-2-olHCID 10998136—

Reaction Steps

A 0° C. solution of (S)—(+)-1,3-butanediol (2.1 g, 23.3 mmol), imidazole (1.74 g, 25.6 mmol), and N,N-dimethylformamide (1.0 mL) in dichloromethane (40 mL) was treated with tert-butyl-dimethylsilyl chloride (3.68 g, 23.3 mmol). The reaction mixture was warmed to room temperature, stirred overnight, quenched with saturated aqueous ammonium chloride and extracted with dichloromethane. The combined dichloromethane layers were dried (MgSO4), filtered and concentrated to afford of the desired product of sufficient purity for subsequent use without further purification in near quantitative yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06559140B2
Source datasetuspto-grants-2003_05
ORD IDord-52f880592c4b40639a7e41c83a8a1b86
Source noteuspto-grants-2003_05