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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9541Generated: October 26, 2026

Hydrochloric Acid → cis-2-(4-Bromobenzoyl)cyclopropanecarboxylic acid

https://huagongshe.com/reaction/9541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBromobenzeneHCID 7961—
Reactant3-Oxabicyclo(3.1.0)hexane-2,4-dioneHCID 2734721—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
Productcis-2-(4-Bromobenzoyl)cyclopropanecarboxylic acidHCID 6714731674.6%

Reaction Steps

To a cold (0° C.) stirred solution of bromobenzene (9.09 g, 57.89 mmol) and AlCl3 (18.36 g, 137.84 mmol) in dry DCM (150 mL) was added 3-oxabicyclo[3.1.0]hexane-2,4-dione (5.40 g, 48.24 mmol). The reaction mixture was stirred at rt for 3 days. The dark-red solution was then poured into ice-cold water (120 mL), and conc. HCl (10 mL) was added. The solution was stirred for few minutes, and the layers were separated. The aqueous layer was extracted with DCM and the combined organic phases were washed with water, brine, dried over Na2SO4 and concentrated to give cis-2-(4-bromobenzoyl)cyclopropanecarboxylic acid (9.69 g, 65%). LC-MS ret. time 2.50; m/z 270 (MH+); 1H NMR (400 MHz, CD2Cl2) δ 1.54 (m, 1H), 1.85 (m, 1H), 2.37 (m, 1H), 2.88 (m, 1H), 7.65 (m, 2H), 7.90 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091228B2
Source datasetuspto-grants-2006_08
ORD IDord-4f34df0009af4ec5b9397ec1a5edea37
Source noteuspto-grants-2006_08