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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809842Generated: November 2, 2026

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

https://huagongshe.com/reaction/1809842

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 numberUS08362003B2
Source datasetuspto-grants-2013_01
ORD IDord-07f113088f9a42ccaa562c9b176f0b69
Source noteuspto-grants-2013_01