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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243215Generated: October 31, 2026

Imidazole → Methyl (3S)-3-(tert-butyldiphenylsilyloxy)-butyrate

https://huagongshe.com/reaction/1243215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
ReactantMethyl 3-hydroxybutyrate, (S)-HCID 6950307—
SolventDichloromethaneHCID 6344—
ProductMethyl (3S)-3-(tert-butyldiphenylsilyloxy)-butyrateHCID 68783265—

Reaction Steps

Methyl (S)-(+)-3-hydroxybutyrate (0.48 g, 4.04 mmol) (Aldrich) was dissolved in dichloromethane (6 mL, dried over molecular sieves). Imidazole (0.39 g, 5.65 mmol) (Aldrich) was added. When all had dissolved, tert-butyldiphenylsilyl chloride (1.05 mL, 4.04 mmol) was added dropwise and the mixture was stirred at room temperature for 4.5 hours. The reaction mixture was diluted with additional dichloromethane, washed with water (2×) and brine, dried over anhydrous sodium sulfate, filtered and concentrated. Purification by flash chromatography (Biotage 40M, 5:95 ethyl acetate-hexanes) gave (S)-3-(tert-butyl-diphenyl-silanyloxy)-butyric acid methyl ester. (Yield 1.33 g, 92.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115740B2
Source datasetuspto-grants-2006_10
ORD IDord-7318163c0f9a4655831e6d9de151afd2
Source noteuspto-grants-2006_10