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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957459Generated: November 4, 2026

Potassium Carbonate → 2-[2-(Tert-butoxycarbonyl)ethyl]-2-ethoxycarbonylcyclohexanone

https://huagongshe.com/reaction/1957459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl acrylateHCID 15458—
ReactantEthyl 2-oxocyclohexanecarboxylateHCID 95543—
SolventDichloromethaneHCID 6344—
Solventtert-ButanolHCID 6386—
Product2-[2-(Tert-butoxycarbonyl)ethyl]-2-ethoxycarbonylcyclohexanoneHCID 19067478—

Reaction Steps

To a solution of 2-ethoxycarbonylcyclohexanone (5.0 g, 0.029 mol) and tert-butyl acrylate (4.83 g, 0.037 mol) in tert-butanol (30 ml) was added, in one portion, potassium carbonate (4.0 g, 0.029 mol). The suspension was stirred at room temperature for 22 hours, diluted with dichloromethane (100 ml) and distilled water (100 ml) and the layers separated. The aqueous layer was extracted with dichloromethane (2×100 ml) and the combined dichloromethane extracts dried over magnesium sulphate, filtered and concentrated under reduced pressure. The residue was purified by chromatography on silica by eluting with hexane/ethyl acetate (4:1) to give, after combination and evaporation of appropriate fractions, the title compound as a colorless oil, (7.99 g, 92.3%; 98.92% by GC normalization) MH+ 299.03, 8.53%). Rf. 0.15 (silica, hexane/ethyl acetate 4:1). 1H-NMR (300 MHz, CDCl3) =1.20 (t, 3H), 1.37 (s, 9H), 1.52-2.46 (m, 12H), 4.08-4.21 (m, 2H) ppm. 13C-NMR (62 MHz, CDCl3) =13.97, 22.38, 27.36, 27.91, 29.52, 30.49, 36.06, 40.85, 59.87, 61.19, 80.10, 171.61, 172.22, 207.39 ppm. Analysis %: Found: C, 64.19; H, 8.80; C16H26O5 requires C, 64.41; H, 8.78.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE035865
Source datasetuspto-grants-1998_07
ORD IDord-b170666a658e4fcea87b68deeae81df9
Source noteuspto-grants-1998_07