Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365647Generated: October 31, 2026

4-tert-Butylcyclohexanone → (4-tert-Butylcyclohexylidene)acetic acid methyl ester

https://huagongshe.com/reaction/365647

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tert-ButylcyclohexanoneHCID 7392—
ReactantAcetic acid, 2-(triphenylphosphoranylidene)-, methyl esterHCID 17453—
SolventTolueneHCID 1140—
Product(4-tert-Butylcyclohexylidene)acetic acid methyl esterHCID 1075095892%

Reaction Steps

4-tert-Butylcyclohexanone (8.62 g, 56 mmol) was dissolved in toluene (200 ml). Methoxycarbonylmethylenetriphenylphosphorane (56.1 g, 168 mmol) was added with stirring and the reaction mixture was heated under reflux for 3 days. The solvent was removed in vacuo. The residue was dissolved in hot hexanes (100 ml) and cooled to room temperature. The precipitate was filtered off and the filtrate was evaporated in vacuo to afford a yellow oil which was then purified by chromatography (silica gel, hexane/ethyl acetate, 2:1 as eluant) to give the title compound as an oil (10.78g, 92%). 1H-NMR; δ (CDCl3) 5.60 (1H, s), 3.87 (1H, m), 3.69 (3H, s), 2.38-2.10 (2H, m), 2.03-1.77 (3H, m), 1.36-1.02 (3H, m) and 0.87 (9H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06127427
Source datasetuspto-grants-2000_10
ORD IDord-c2fff63f000a41038e0d051d0a83e5ba
Source noteuspto-grants-2000_10