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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732022Generated: October 25, 2026

Carbon Dioxide → 3-Cyclopropylbenzoic acid

https://huagongshe.com/reaction/732022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
Reactant1-Bromo-3-cyclopropylbenzeneHCID 3282672—
ReactantButyllithiumHCID 178418339—
Product3-Cyclopropylbenzoic acidHCID 282065—

Reaction Steps

1.6 M n-Butyllithium in hexanes (3.2 mL, 5.1 mmol) was added drop-wise to a solution of 1-bromo-3-cyclopropyl-benzene at −78° C. and stirred for 1 hour. This reaction mixture was then transferred via canula to a 250 mL round bottom flask equipped with a stirrer bar approximately ¼ full of solid carbon dioxide and stirred and for 1 hour. The reaction mixture was concentrated and then the residue was diluted with water. The aqueous layer was washed with dichloromethane (3×), acidified with 1 N HCl to pH˜2, and extracted with ethyl acetate. The organic phase was washed with water and saturated brine, dried over anhydrous sodium sulfate, filtered and concentrated to afford 3-cyclopropyl-benzoic (356 mg, 43%, white solid).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585881B2
Source datasetuspto-grants-2009_09
ORD IDord-2b2875ec77e54f688239d75101e02be0
Source noteuspto-grants-2009_09