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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2268749Generated: October 30, 2026

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

https://huagongshe.com/reaction/2268749

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 vacua. 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 (10.78 g, 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 numberUS06329373B1
Source datasetuspto-grants-2001_12
ORD IDord-932310a3fc7a4940abc23daa890f1fff
Source noteuspto-grants-2001_12