Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173181Generated: October 26, 2026

Imidazole → cis-4-((t-Butyldimethylsilyl)oxy)cyclohexan-1-ol

https://huagongshe.com/reaction/1173181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantTriethylamineHCID 8471—
Reactant1,4-CyclohexanediolHCID 11162—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Productcis-4-((t-Butyldimethylsilyl)oxy)cyclohexan-1-olHCID 55453942.4%

Reaction Steps

To a solution of 1,4-cyclohexanediol (5 g, 43 mmol), imidazole (2.92 g, 43 mmol) and NEt3 (7 mL) in CH2Cl2 (100 mL) cooled in an ice bath was added tert-butyldimethylsilyl chloride (6.47 g, 43 mmol). The mixture was stirred at room temperature overnight. Water was added and the organic phase was separated. The aqueous layer was extracted with EtOAc. The combined organic phase was dried over MgSO4 and concentrated. Chromatography on silica gel eluting with 3:1 EtOAc/hexanes provided the title compound (4.2 g, 42%) as an oil. MS calculated (M+H)+ 231, found 231.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834021B2
Source datasetuspto-grants-2010_11
ORD IDord-c8816731a86148869c9f53f8a24c26a3
Source noteuspto-grants-2010_11