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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768709Generated: October 31, 2026

Sulfur Dioxide → 2-aminosulfonyl-6-sec-butyl-4-methoxy-N,N-diethylbenzamide

https://huagongshe.com/reaction/1768709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfur DioxideHCID 1119—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantAmmonium HydroxideHCID 14923—
ReactantSulfuryl chlorideHCID 24648—
Reactant2-sec-butyl-4-methoxy-N,N-diethylbenzamideHCID 19373058—
ReactantCID 53628100HCID 178418400—
SolventTetrahydrofuranHCID 8028—
Product2-aminosulfonyl-6-sec-butyl-4-methoxy-N,N-diethylbenzamideHCID 19373057—

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a solution of tetramethylethylenediamine (31 mL) in THF (500 mL) at -78° C. was added sec-butyllithium (170 mL, 1.1M), followed by 2-sec-butyl-4-methoxy-N,N-diethylbenzamide (45 g) in THF (150 mL). The mixture was stirred at -78° for 15 minutes, then at 0° C. for 30 minutes, then sulfur dioxide (50 mL) was condensed into the mixture at -78° C. The mixture was warmed to -10° C., sulfuryl chloride (17 mL) was added and then the mixture was slowly warmed to room temperature and stirred overnight. The reaction mixture was added to a solution of ammonium hydroxide (94 mL) in THF (200 mL), the mixture was filtered through a pad of silica/Na2SO4 /sand to afford 51.8 g of 2-aminosulfonyl-6sec-butyl-4-methoxy-N,N-diethylbenzamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05378720
Source datasetuspto-grants-1995_01
ORD IDord-48466708a3e142baac4c8844a95e6aa7
Source noteuspto-grants-1995_01