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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177260Generated: October 31, 2026

Methanesulfonyl chloride → HCID 90418627, compound

https://huagongshe.com/reaction/2177260

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 90418369HCID 90418369—
SolventDichloromethaneHCID 6344—
ProductHCID 90418627HCID 90418627—

Reaction Conditions

Temperature20 °C

Reaction Steps

Into a 25-mL round-bottom flask, was placed (3-chloro-5-phenyl-1,2-thiazol-4-yl)methanol (80 mg, 0.34 mmol, 1.00 equiv, 97%), MsCl (81.6 mg, 0.72 mmol, 2.00 equiv), TEA (107.7 mg, 1.06 mmol, 3.00 equiv), dichloromethane (1.5 mL). The resulting solution was stirred for 1 h at 20° C. The reaction was then quenched by the addition of 5 mL of water. The resulting solution was extracted with 3×5 mL of ethyl acetate and the organic layers combined and dried over anhydrous sodium sulfate. The solids were filtered out. The resulting mixture was concentrated under vacuum. This resulted in 85 mg (96%) of 3-chloro-4-(chloromethyl)-5-phenyl-1,2-thiazole as yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067898B1
Source datasetuspto-grants-2015_06
ORD IDord-c0b7775c7a164a3091e94f122c6f73f0
Source noteuspto-grants-2015_06