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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559505Generated: October 29, 2026

Chloromethyl Methyl Ether → 4-cyano-N-methoxymethyl-N-thiazol-2-yl-benzenesulfonamide

https://huagongshe.com/reaction/559505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantPotassium CarbonateHCID 11430—
Reactant4-cyano-N-(thiazol-2-yl)benzenesulfonamideHCID 24705026—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-cyano-N-methoxymethyl-N-thiazol-2-yl-benzenesulfonamideHCID 6700144782%

Reaction Steps

To a suspension of 4-cyano-N-thiazol-2-yl-benzenesulfonamide (10 mmol) and potassium carbonate (15 mmol) in DMF (30 mL) was added chloro-methoxy-methane (10 mmol) and the mixture was stirred for 4 h. The reaction mixture was diluted with water (30 mL) and the resulting mixture was extracted with ethyl acetate. The organic phase was washed with brine, dried over MgSO4, and concentrated in vacuo. The crude product was purified by column chromatography to give 4-cyano-N-methoxymethyl-N-thiazol-2-yl-benzenesulfonamide (8.2 mmol) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063080B2
Source datasetuspto-grants-2011_11
ORD IDord-deb68dad50a94059a400e70fe4682505
Source noteuspto-grants-2011_11