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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357423Generated: November 1, 2026

Imidazole → tert-butyl (3S,7R,8S)-5-oxo-3-(triethylsilyloxy)-4,4,8-trimethyl-7-(2,2,2-trichloroethoxy-carbonyloxy)-10-undecenoate

https://huagongshe.com/reaction/1357423

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantWaterHCID 962—
ReactantChlorotriethylsilaneHCID 13819—
Reactanttert-butyl (3S,7R,8S)-5-oxo-3-hydroxy-4,4,8-trimethyl-7-(2,2,2-trichloroethoxycarbonyloxy)-10-undecenoateHCID 60003397—
SolventDimethylformamideHCID 6228—
Producttert-butyl (3S,7R,8S)-5-oxo-3-(triethylsilyloxy)-4,4,8-trimethyl-7-(2,2,2-trichloroethoxy-carbonyloxy)-10-undecenoateHCID 86586621—

Reaction Steps

A solution of tert-butyl (3S,7R,8S)-5-oxo-3-hydroxy-4,4,8-trimethyl-7-(2,2,2-trichloroethoxycarbonyloxy)-10-undecenoate (1.7 g), imidazole (0.48 g), and triethylsilyl chloride (0.68 g) in 5 mL of dimethylformamide is stirred for 2 hours at ambient temperature, then poured into water and extracted with ether. The extract is washed with sat. aq. NaCl, dried over MgSO4, filtered, and evaporated. The product is purified by chromatography on SiO2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06589968B2
Source datasetuspto-grants-2003_07
ORD IDord-14507e6710d34ce0abbff3aa5c1cf785
Source noteuspto-grants-2003_07