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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087218Generated: October 31, 2026

Triethylamine → HCID 10338212, compound

https://huagongshe.com/reaction/1087218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 10446139HCID 10446139—
SolventPyridineHCID 1049—
ProductHCID 10338212HCID 10338212—

Reaction Steps

Methanesulfonyl chloride (2.2 ml) was added dropwise to an ice-cooled solution of 4-amino-5-(2,4-difluorophenylthio)-2-methylbenzonitrile (3.9 g) and triethylamine (3.9 ml) in pyridine (40 ml). The mixture was stirred overnight at room temperature and concentrated to dryness. To the residue were added pyridine (10 ml) and 5% aqueous solution of sodium hydroxide (50 ml). The resulting mixture was stirred for 2 hours and washed with toluene (50 ml). The aqueous layer was acidified with hydrochloric acid, and the precipitates obtained were recrystallized from a mixture of ethanol and ethyl acetate to give a pale brown powder of 4'-cyano-2'-(2,4-difluorophenylthio)-5'-methylmethanesulfonanilide (2.6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05034417
Source datasetuspto-grants-1991_07
ORD IDord-b3f5e76754cf4c099795ecb13ab1296f
Source noteuspto-grants-1991_07