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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642745Generated: October 25, 2026

Benzoyl chloride → 6-Oxobicyclo[3.2.0]heptan-2-yl benzoate

https://huagongshe.com/reaction/642745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
Reactant2-Hydroxybicyclo[3.2.0]heptan-6-oneHCID 13443807—
SolventDichloromethaneHCID 6344—
Product6-Oxobicyclo[3.2.0]heptan-2-yl benzoateHCID 5925957586.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of compound 1G (1.9 g, 15.1 mmol) in CH2Cl2 (10 mL) at 0° C. under nitrogen were added Et3N (3.1 mL, 22.2 mmol) and benzoyl chloride (2.33 g, 16.6 mmol). The reaction was stirred at 0° C. for 60 min and RT for 30 min, then quenched with water. The product was extracted with CH2Cl2, the organics were washed with saturated aqueous NaHCO3, dried over Na2SO4, and concentrated. Purification by silica gel chromatography (5% EtOAc in hexanes) provide the title compound (3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696241B2
Source datasetuspto-grants-2010_04
ORD IDord-702fd5351b1f45cbbfb37422ed9dc037
Source noteuspto-grants-2010_04