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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956382Generated: November 2, 2026

3-Cyclohexene-1-methanol → HCID 53968181, compound

https://huagongshe.com/reaction/1956382

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Cyclohexene-1-methanolHCID 15512—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
ProductHCID 53968181HCID 53968181—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a mixture of 3-cyclohexene-1-methanol (Aldrich, 13.0 mL, 0.11 mol), N,N-diisopropylethylamine (43 mL, 0.244 mol) and 4-dimethylaminopyridine (2.70 g., 0.022 mol) in 375 mL of dry CH2CI2 under N2 at 25° C. was added tert-butyldiphenylchlorosilane (32 mL, 0.123 mol). The mixture was stirred at 25° C. for 48 hours. The reaction mixture was washed sequentially with 150 mL portions of 1N HCl, water, brine and dried over anhydrous MgSO4. The solvent was evaporated. The residue was loaded onto a 4"×4"column of silica and slowly eluted using hexanes as eluant. 3-(tert-butyldiphenylsilyloxymethylene)-1-cyclohexene, 33.6 g (86%), was obtained as a colorless oil which was homogenous by TLC (Rf=0.4, hexanes). Analytical calculated for C23H30OSi(0.3 H2O): C, 77.6; H 8.67. Found: C, 77.38; H, 8.72.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05780461
Source datasetuspto-grants-1998_07
ORD IDord-72c654ba06a34b18975f290902f9a24b
Source noteuspto-grants-1998_07