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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902850Generated: October 26, 2026

Benzyl Bromide → Benzyl 3-oxocyclobutane-1-carboxylate

https://huagongshe.com/reaction/902850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantTriethylamineHCID 8471—
Reactant3-Oxocyclobutane-1-carboxylic acidHCID 4913358—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductBenzyl 3-oxocyclobutane-1-carboxylateHCID 15830669—

Reaction Steps

Triethylamine (2.0 ml) and benzyl bromide (1.2 ml) were added to a solution of 3-oxocyclobutanecarboxylic acid (J. Org. Chem., Vol. 53, pp. 3841-3843, 1981) (995 mg) in tetrahydrofuran (5.0 ml), and the mixture was stirred at room temperature for 2 hours. The reaction mixture was diluted with ethyl acetate, and washed successively with 1N hydrochloric acid, a saturated aqueous solution of sodium hydrogencarbonate and saturated saline and dried over anhydrous sodium sulfate. The solvent was then distilled off under reduced pressure, and the resultant residue was purified by column chromatography on silica gel (ethyl acetate:hexane=1:6) to obtain the title compound (886 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07365205B2
Source datasetuspto-grants-2008_04
ORD IDord-07c3e1a107444d588f764371b11c5688
Source noteuspto-grants-2008_04