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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1680263Generated: October 30, 2026

Benzoyl chloride → HCID 54109752, compound

https://huagongshe.com/reaction/1680263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantMethyl 2,3-dihydro-6-methoxy-1H-indene-1-carboxylateHCID 14843791—
SolventDichloromethaneHCID 6344—
ProductHCID 54109752HCID 54109752—

Reaction Steps

40 g of finely powdered aluminium chloride are added in portions to a stirred solution of 20.6 g of 6-methoxy-indane-1-carboxylic acid methyl ester and 15.5 g of benzoyl chloride in 200 ml of absolute methylene chloride at 20° C., in an anhydrous atmosphere, stirring is continued overnight at room temperature and the reaction solution is then poured onto 500 g of ice and extracted with 3 times 100 ml of methylene chloride. The organic phases are washed successively with 500 ml of saturated sodium bicarbonate solution, 500 ml of 2 N hydrochloric acid and 500 ml of water, dried over anhydrous sodium sulphate and evaporated in vacuo. The evaporation residue, when crystallised from ether-petroleum ether after treatment with active charcoal, gives 5-benzoyl-6-hydroxy-indane-1-carboxylic acid methyl ester of melting point 89°-91° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04272547
Source datasetuspto-grants-1981_06
ORD IDord-d89173f0fe0f45be8ead242a1b5dd5e5
Source noteuspto-grants-1981_06