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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35501Generated: October 28, 2026

Acetyl chloride → N,N-dimethyl-3-methyl-4-(N-acetyl-N-trifluoromethanesulfonylamino)benzenesulfonamide

https://huagongshe.com/reaction/35501

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
ReactantN,N-dimethyl-3-methyl-4-(trifluoromethanesulfonamido)benzenesulfonamideHCID 13422930—
SolventTetrahydrofuranHCID 8028—
ProductN,N-dimethyl-3-methyl-4-(N-acetyl-N-trifluoromethanesulfonylamino)benzenesulfonamideHCID 1342296376.7%

Reaction Steps

To a solution of N,N-dimethyl-3-methyl-4-(trifluoromethanesulfonamido)benzenesulfonamide (1.5 g) and triethylamine (0.65 g) in tetrahydrofuran (40 ml), acetyl chloride (0.51 g) was added, and the resultant mixture was stirred at room temperature for 3 hours. The reaction mixture was concentrated and solidified with water. The solidified product was recrystallized from a mixture of ethanol and toluene to give 1.29 g of N,N-dimethyl-3-methyl-4-(N-acetyl-N-trifluoromethanesulfonylamino)benzenesulfonamide (Compound No. 86). M.P., 148°-148.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04767446
Source datasetuspto-grants-1988_08
ORD IDord-bb437d8d7be3488c969f694be9edb1e1
Source noteuspto-grants-1988_08