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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181768Generated: 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/2181768

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 numberUS06893859B2
Source datasetuspto-grants-2005_05
ORD IDord-2108dd2d894441b6a970527f721227fd
Source noteuspto-grants-2005_05