Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616637Generated: October 29, 2026

Benzoyl chloride, 3-chloro- → HCID 20368321, compound

https://huagongshe.com/reaction/616637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chloride, 3-chloro-HCID 69252—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 15422638HCID 15422638—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 20368321HCID 20368321—

Reaction Conditions

Temperature0 °C

Reaction Steps

To 200 ml. of 1,2-dichloroethane were added 10.0 g. (0.042 mole) of 3-phenyl-6-methoxybenzothiophene and 6.5 g. (0.042 mole) of 3-chlorobenzoyl chloride. The mixture was stirred and cooled to 0° C., and 5.73 g. (0.042 mole) of aluminum chloride were added. The mixture was stirred for about one hour and ice then was added. The resulting organic layer was separated from the aqueous. The aqueous layer was washed with chloroform, and the chloroform was separated and added to the organic layer. The organic layer then was evaporated, and to the resulting residue were added 250 ml. of methanol and 15 ml. of 5N sodium hydroxide. The mixture was refluxed for 30 minutes and evaporated. The residue was recrystallized from methanol to obtain the title compound, m.p. 105° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04075227
Source datasetuspto-grants-1978_02
ORD IDord-a28d64416f574db4884450a520c8a978
Source noteuspto-grants-1978_02