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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605517Generated: October 26, 2026

Potassium bis(trimethylsilyl)amide → Methyl 4-vinylbicyclo[2.2.2]octane-1-carboxylate

https://huagongshe.com/reaction/605517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantMethyl 4-formylbicyclo[2.2.2]octane-1-carboxylateHCID 11074324—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductMethyl 4-vinylbicyclo[2.2.2]octane-1-carboxylateHCID 22591686—

Reaction Steps

To a stirred solution of methyltriphenylphosphonium bromide (9.1 g, 12.8 mmol) in THF (50 ml) at 0° C. was added potassium hexamethyldisilazide (0.5M in toluene, 48.6 ml), dropwise over 5 min. The resulting mixture was allowed to warm up to room temperature over 1 h, then cooled again to 0° C. and treated with methyl 4-formylbicyclo[2.2.2]octane-1-carboxylate (4-1) (Chapman, N. B. et al. J. Org. Chem., 1970, 35, 917) (2.5 g, 12.8 mmol). The reaction mixture was stirred at room temperature for 18 h then diluted with EtOAc (350 ml). The organic phase was washed with aqueous HCl (1 N), saturated aqueous sodium bicarbonate, and brine, then dried (Na2SO4) and concentrated in vacuo. The resulting solid was purified by flash silica gel chromatography, eluting with a gradient 0-4% EtOAc/hexanes. The resulting methyl 4-vinylbicyclo[2.2.2]octane-1-carboxylate (4-2) was isolated as a clear, colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915252B2
Source datasetuspto-grants-2011_03
ORD IDord-a249cc4f4a3f44159580afdaa560d2b8
Source noteuspto-grants-2011_03