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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 864721Generated: October 31, 2026

Sulfur Dioxide → HCID 14984039, compound

https://huagongshe.com/reaction/864721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfur DioxideHCID 1119—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
Reactanthydroxylamine-O-sulfonic acidHCID 76284—
ReactantN,N-diethyl-2-methoxybenzamideHCID 346975—
ReactantSodium AcetateHCID 517045—
ReactantCID 53628100HCID 178418400—
SolventTetrahydrofuranHCID 8028—
SolventCyclohexaneHCID 8078—
ProductHCID 14984039HCID 1498403949%

Reaction Steps

To a solution of 8.0 ml (0.053 mol) of tetramethylethylenediamine (TMEDA) in 350 ml of THF at -70° C. was added 42 ml (0.055 mol) of a 1.3M solution of s-butyl lithium in cyclohexane and the mixture was stirred for fifteen minutes. To the solution was added dropwise with stirring a solution of 10.36 g (0.050 mol) of 2-methoxy-N,N-diethylbenzamide in 150 ml of THF while maintaining the temperature at -60° C. or below. After stirring for 20 minutes sulfur dioxide was bubbled into the reaction mixture, keeping the reaction temperature below -50° C. until the reaction mixture was acid to wet litmus paper. The mixture was stirred at ambient temperature for two hours, diluted with 450 ml of hexane, and the solid material which had separated was collected, dissolved in 200 ml of water and the mixture treated with 65 g of sodium acetate and 21.5 g (0.19 mol) of hydroxylamine-O-sulfonic acid in portions with stirring. The white solid which separated was collected and dried to give 7.04 g (49%) of 2-aminosulfonyl-6-methoxy-N,N-diethylbenzamide, mp 190°-194.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05563163
Source datasetuspto-grants-1996_10
ORD IDord-e11bf61e08cb4aa39a2f6c186fa8e97e
Source noteuspto-grants-1996_10