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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296868Generated: October 31, 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/2296868

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 numberUS06489314B1
Source datasetuspto-grants-2002_12
ORD IDord-5c0ba393c4cb4d90bb7ca8def80be6b9
Source noteuspto-grants-2002_12