Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167431Generated: November 1, 2026

Thionyl Chloride → HCID 86584468, compound

https://huagongshe.com/reaction/2167431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 86584469HCID 86584469—
SolventDichloromethaneHCID 6344—
ProductHCID 86584468HCID 86584468—

Reaction Steps

A mixture of 6.9 g (20 mmol) of methyl 2-chloro-3-(1′-hydroxy-2′,2′-dimethylethylaminocarbonyl)-4-methylsulfonylbenzoate and 5 ml of thionyl chloride was stirred for 6 hours at room temperature. The solution was diluted with 50 ml of dichloromethane and subsequently concentrated. The residue was dissolved in 20 ml of dichloromethane. The addition of cyclohexane resulted in a crystalline precipitate which was filtered off with suction and dried. This gave 6.4 g (88% of theory) of methyl 2-chloro-3-(1′-chloro-2′,2′-dimethylethylaminocarbonyl)-4-methylsulfonylbenzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045465B1
Source datasetuspto-grants-2015_06
ORD IDord-bc2db9591b4c433d835ada54c0d1a16e
Source noteuspto-grants-2015_06