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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786282Generated: October 31, 2026

Benzyl Alcohol → Benzyl 3-methylidenecyclobutane-1-carboxylate

https://huagongshe.com/reaction/1786282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
SolventDiethyl EtherHCID 3283—
SolventEthyl AcetateHCID 8857—
ProductBenzyl 3-methylidenecyclobutane-1-carboxylateHCID 57478428115.2%

Reaction Steps

A suspension of 1,1′-carbonyldiimidazole (1.59 g, 9.81 mmol) in ethyl acetate (5 ml) was added in portions to a solution of the product of Preparation 12 (1 g, 8.9 mmol) in ethyl acetate (5 ml). Gentle effervescence was observed. The mixture was stirred at room temperature for about 1.5 hours, benzyl alcohol (1.11 ml, 10.7 mmol) added and stirring continued overnight. The solution was diluted with diethyl ether (20 ml), washed with water (2×10 ml), dried over magnesium sulphate and evaporated in vacuo to a colourless liquid which was purified by filtering through 10 g SiO2, eluting with dichloromethane, to give the title compound as a colourless oil (1.246 g, 69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507742B2
Source datasetuspto-grants-2009_03
ORD IDord-e1b73198fb504a57abdf39bd7fa3a0f2
Source noteuspto-grants-2009_03