Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2163316Generated: October 31, 2026

1,2-Dichloroethane → [6-Methoxy-2-(4-methoxyphenyl)-1-benzothiophen-3-yl](phenyl)methanone

https://huagongshe.com/reaction/2163316

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantBenzoyl chlorideHCID 7412—
Reactant6-Methoxy-2-(4-methoxyphenyl)benzo[b]thiopheneHCID 850941—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventWaterHCID 962—
Product[6-Methoxy-2-(4-methoxyphenyl)-1-benzothiophen-3-yl](phenyl)methanoneHCID 22753379—

Reaction Steps

To 300 ml. of 1,2-dichloroethane maintained at 0° C. were added 6.0 g. (0.022 mole) of 2-(4-methoxyphenyl)-6-methoxybenzothiophene and 3.10 g. (0.022 mole) of benzoyl chloride. The mixture was stirred vigorously, and 3.2 g. (0.024 mole) of aluminum chloride were added in small portions. The resulting red solution was stirred for one hour, and water then was added. The yellow organic layer was separated, washed with 200 ml. of 1N sodium hydroxide and then with 200 ml. of saturated sodium chloride solution. The mixture then was dried over potassium carbonate, and the solvent was evaporated to give a pale yellow solid which was purified by chromatography over silica gel using benzene and 5% ethyl acetate in benzene as eluant. The appropriate fractions gave product as yellow crystals. The product was recrystallized from methanol to obtain 3.5 g. (42 percent) of 2-(4-methoxyphenyl)-3-benozyl-6-methoxybenzothiophene, melting point 110.5°-111° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04133814
Source datasetuspto-grants-1979_01
ORD IDord-195e3913920d4ab8ad8e73af3017a1a7
Source noteuspto-grants-1979_01