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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177271Generated: October 29, 2026

Methanesulfonyl chloride → 3-Chloro-4-(chloromethyl)-5-(4-methoxyphenyl)-1,2-thiazole

https://huagongshe.com/reaction/2177271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant[3-Chloro-5-(4-methoxyphenyl)-1,2-thiazol-4-yl]methanolHCID 90418060—
SolventDichloromethaneHCID 6344—
Product3-Chloro-4-(chloromethyl)-5-(4-methoxyphenyl)-1,2-thiazoleHCID 90418320—

Reaction Conditions

Temperature0 °C

Reaction Steps

Into a 100-mL round-bottom flask, was placed [3-chloro-5-(4-methoxyphenyl)-1,2-thiazol-4-yl]methanol (223 mg, 0.87 mmol, 1.00 equiv), dichloromethane (20 mL), TEA (261 mg, 2.58 mmol, 2.96 equiv). This was followed by the addition of MsCl (200 mg) dropwise with stirring at 0° C. The resulting solution was stirred for 2 h at room temperature. The resulting solution was diluted with 40 mL of DCM. The resulting mixture was washed with 3×10 mL of water. The mixture was dried over anhydrous sodium sulfate and concentrated under vacuum. This resulted in 430 mg (crude) of 3-chloro-4-(chloromethyl)-5-(4-methoxyphenyl)-1,2-thiazole as yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067898B1
Source datasetuspto-grants-2015_06
ORD IDord-254f3024b4774307a24347037bc0d96a
Source noteuspto-grants-2015_06