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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903465Generated: November 1, 2026

Thionyl Chloride → 6,7-dichloro-5-methoxy-2-isopropylbenzo[b]thiophen-3(2H)-one

https://huagongshe.com/reaction/1903465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant2-[(2,3-Dichloro-4-methoxyphenyl)sulfanyl]-3-methylbutanoic acidHCID 15914270—
SolventDichloromethaneHCID 6344—
Product6,7-dichloro-5-methoxy-2-isopropylbenzo[b]thiophen-3(2H)-oneHCID 2019793545%

Reaction Steps

To 6.0 g of α-(2,3-dichloro-4-methoxyphenylthio)isovaleric acid in 27 ml of dry dichloromethane is added 5.5 ml of thionyl chloride. The reaction is heated under reflux for 1 hour and excess reagent is removed under aspirator pressure. The residue is diluted with 70 ml of dichloromethane and the resulting slurry is added over less than one minute to a slurry of 2.79 g of aluminum chloride in 8 ml of dichloromethane at -60°. The cooling bath is removed and the reaction allowed to warm to room temperature over one hour. Stirring is continued for an additional hour and reaction is quenched with 250 ml of water. The mixture is extracted with three 125 ml portions of ether and the combined ether extracts are washed with two 150 ml portions and one 60 ml portion of saturated sodium bicarbonate solution, water and brine and dried over anhydrous magnesium sulfate to give 2.54 g of oily 6,7-dichloro-5-methoxy-2-isopropylbenzo[b]thiophen-3(2H)-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04436748
Source datasetuspto-grants-1984_03
ORD IDord-1ff81eacfce440ba8c6de8b91772566e
Source noteuspto-grants-1984_03