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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720173Generated: October 25, 2026

Hydrochloric Acid → Ethyl 2-(4-n-octylbenzoyl)cyclopropane carboxylate

https://huagongshe.com/reaction/1720173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantOctylbenzeneHCID 16607—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 12547528HCID 12547528—
SolventDichloromethaneHCID 6344—
ProductEthyl 2-(4-n-octylbenzoyl)cyclopropane carboxylateHCID 2242039660.3%

Reaction Steps

Aluminum chloride (6.93 g) is added in one portion to a solution of 2-ethoxycarbonyl-cyclopropane carboxylic acid chloride (4.17 g) and 1-phenyloctane (4.49 g) in methylene chloride (100 ml). After the initial exothermic reaction subsides, the mixture is heated under reflux for 16 hours. The mixture is cooled and poured into ice water (500 ml) containing conc. hydrochloric acid (50 ml). The product is extracted with ether (3×200 ml). The extract is dried over MgSO4 and then evaporated under reduced pressure. The residue is chromatographed on silica gel (hexane/ether) to provide ethyl 2-(4-n-octylbenzoyl)cyclopropane carboxylate as an oil (4.7 g). This ester is heated under reflux in aqueous 2N NaOH (36 ml) for 24 hours. The reaction mixture is diluted with water (100 ml), acidified and extracted with ether (3×50 ml). The extract is dried (MgSO4) and evaporated. The residue is crystallized from petroleum ether (40°-60°) to provide 2-(4-n-octylbenzoyl) cyclopropane carboxylic acid (1.88 g), m.p. 45°-47° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05504244
Source datasetuspto-grants-1996_04
ORD IDord-051752b37ef14308b1dc2ca8a4e689fc
Source noteuspto-grants-1996_04