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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098136Generated: October 26, 2026

Imidazole → Methyl 5-(tert-butyl-dimethylsilyl)oxypentanoate

https://huagongshe.com/reaction/1098136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantPentanoic acid, 5-hydroxy-, methyl esterHCID 3014818—
SolventDichloromethaneHCID 6344—
ProductMethyl 5-(tert-butyl-dimethylsilyl)oxypentanoateHCID 1113943252%

Reaction Steps

A solution of tert-butylchlorodimethylsilane (27.1 g, 179.79 mmol) in DCM (50 mL) was added dropwise to a stirred solution of methyl 5-hydroxypentanoate (CAS no. 14273-92-8, Huckstep, M.; Taylor, R. J. K.; Caton, M. P. L. Synthesis 1982, 10, 881) (19.8 g, 149.82 mmol) and 1H-imidazole (15.30 g, 224.73 mmol) in DCM (200 mL) at 5° C., over a period of 10 minutes under nitrogen. The resulting suspension was stirred at ambient temperature for 6 hours. The reaction mixture was diluted with DCM (250 mL), and washed sequentially with water (2×200 mL) and saturated brine (200 mL). The organic layer was dried (MgSO4) and evaporated. The residue was purified by flash silica chromatography, eluting with 10 to 50% ethyl acetate in isohexane to afford the product (19.3 g, 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143263B2
Source datasetuspto-grants-2012_03
ORD IDord-c3e8a6411ea7432b85eed9fffce967b1
Source noteuspto-grants-2012_03