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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1180656Generated: October 27, 2026

Hydrochloric Acid → 5-Methylbenzo[b]thiophene-2-sulfonamide

https://huagongshe.com/reaction/1180656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAmmonium HydroxideHCID 14923—
ReactantSulfuryl chlorideHCID 24648—
Reactant5-Methylbenzo(b)thiopheneHCID 84346—
ReactantButyllithiumHCID 178418339—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product5-Methylbenzo[b]thiophene-2-sulfonamideHCID 1392286616%

Reaction Conditions

Temperature0 °C

Reaction Steps

5-Methyl-benzo[b]thiophene (220 mg, 1.5 mmol) is dissolved in dry THF (1.5 mL) and cooled to 0° C. To this solution is slowly added 1.6 M n-BuLi in hexane (1.0 mL, 1.6 mmol) and the temperature maintained at 0° C. and the reaction mixture stirred for 20 min. Then the heterogeneous mixture is diluted with 2 mL of THF and transferred by canula to a well-stirred solution of sulfuryl chloride (245 μL, 4.6 mmol) in hexane (1.5 mL) at 0° C. After 1 hr, the suspension is diluted with acetone and the resulting solution of acid chloride is added slowly to a solution of 2 mL of NH4OH in acetone (5 mL). The mixture is diluted with water and acidified with conc. HCl. The aqueous solution is acidified and the product is extracted into ethyl acetate. The organic phase is washed with water and brine, dried (Na2SO4), and evaporated. The crude product is purified by silica gel chromatography (eluent: hexane 3/ethyl acetate 1) to afford the title compound (53 mg, 16%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07282595B2
Source datasetuspto-grants-2007_10
ORD IDord-64e5204956f14aac8b1cc3bfa721080f
Source noteuspto-grants-2007_10