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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1970982Generated: November 3, 2026

Water → {[4-(Benzyloxy)cyclohex-1-en-1-yl]oxy}(tert-butyl)dimethylsilane

https://huagongshe.com/reaction/1970982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyldimethylsilyl trifluoromethanesulphonateHCID 123564—
Reactant4-(Benzyloxy)cyclohexanoneHCID 10987369—
SolventDichloromethaneHCID 6344—
Product{[4-(Benzyloxy)cyclohex-1-en-1-yl]oxy}(tert-butyl)dimethylsilaneHCID 68669646—

Reaction Steps

To a stirred solution of 4-(benzyloxy)cyclohexanone (10 g, 49 mmol) and Hunig's base (17.1 mL, 98 mmol) in DCM (50 mL) was added TBSOTf (11.8 mL, 51.4 mmol) in DCM (50 mL) dropwise at 0° C. The reaction mixture was allowed to warm to room temperature, and left to stir until the reaction was complete. The mixture was poured into water, and the organic layer was separated, dried, and concentrated. Purification by flash chromatography afforded the title compound. 1H NMR (600 MHz, CDCl3) δ 7.20-7.36 (m, 5H); 4.72 (br s, 1H); 4.55 (s, 2H); 3.60 (m, 1H); 1.72-2.38 (series of m, 6H); 0.90 (s, 9H); 0.10 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431569B2
Source datasetuspto-grants-2013_04
ORD IDord-96fc2d9eab53417196588f7400fcbad0
Source noteuspto-grants-2013_04