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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 816Generated: October 23, 2026

Hydrochloric Acid → N-(1,1-Dimethylethyl)-1-methyl-2-(methylthio)-1H-pyrrole-3-sulfonamide

https://huagongshe.com/en/reaction/816

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethyl DisulfideHCID 12232—
ReactantN-(1,1-Dimethylethyl)-1-methyl-1H-pyrrole-3-sulfonamideHCID 19693811—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductN-(1,1-Dimethylethyl)-1-methyl-2-(methylthio)-1H-pyrrole-3-sulfonamideHCID 1969381458.8%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 6.48 g (30 mmol) of N-(1,1-dimethylethyl)-1-methyl-1H-pyrrole-3-sulfonamide in 150 mL THF under nitrogen atmosphere cooled to -78° C. was added dropwise at such a rate as to keep the temperature below -65° C. 25.52 mL (61.5 mmol) 2.41M n-butyllithium in hexanes. The reaction was stirred at -78° C. for ca. 30 minutes. To the reaction mixture was added 2.97 mL (33 mmol) of dimethyldisulfide in one portion and the resulting reaction mixture was allowed to warm to room temperature and stir for ca. 1.5 hours. The reaction mixture was cooled to 0° C. and acidified with 1N HCl. The THF phase was separated washed with brine, dried (MgSO4) and concentrated in vacuo. The crude residue was chromatographed on silica (20% ethyl acetate/80% hexanes) affording 4.63 g of the title compound as an off white solid, m.p. 116°-119° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05723410
Source datasetuspto-grants-1998_03
ORD IDord-ec291f168e3d4ab6bc17d0209ef33361
Source noteuspto-grants-1998_03