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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32855Generated: October 29, 2026

Imidazole → 1,2,3,6-Tetrahydrobenzylalcohol, tert-butyldimethylsilyl ether

https://huagongshe.com/reaction/32855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactant3-Cyclohexene-1-methanolHCID 15512—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
Product1,2,3,6-Tetrahydrobenzylalcohol, tert-butyldimethylsilyl etherHCID 11229886100%

Reaction Steps

To a stirred solution of 1,2,3,6-tetrahydrobenzylalcohol (1) (1.12 g, 10 mmol) and imidazole (1.36 g, 20 mmol) in DMF (10 mL) was added TBDMSCl (1.81 g, 12 mmol). After 20 hours, the mixture was treated with brine (100 mL) and the product was extracted with hexanes (3×80 mL). The combined organic layers were washed with brine (100 mL), dried over MgSO4 and evaporated in vacuo to give compound (2) (2.26 g, 100%) as colorless liquid. Rf0.29 (hexanes). 1H NMR (CDCl3) δ 5.65-5.64 (m, 2H), 3.48 (d, J=2.3 Hz, 1H), 3.45 (d, J=2.3 Hz, 1H), 2.08-2.00 (m, 3H), 1.82-1.66 (m, 3H), 1.32-1.19 (m, 1H), 0.89 (s, 9H), 0.04 (s, 6H); 13C NMR (CDCl3) δ 127.04, 126.23, 67.95, 36.34, 28.23, 25.97, 25.70, 25.33, 24.78, 18.38, −5.32.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07427678B2
Source datasetuspto-grants-2008_09
ORD IDord-396347309c7e45c5aa561df64ccbeaed
Source noteuspto-grants-2008_09