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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34869Generated: October 28, 2026

Iodobenzene → N-(1,1-dimethylethyl)-2-(methylthio)-6-phenylbenzenesulfonamide

https://huagongshe.com/reaction/34869

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodobenzeneHCID 11575—
ReactantAmmonium HydroxideHCID 14923—
ReactantN-(1,1-dimethylethyl)-2-(methylthio)benzenesulfonamideHCID 13670364—
ReactantButyllithiumHCID 178418339—
SolventAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductN-(1,1-dimethylethyl)-2-(methylthio)-6-phenylbenzenesulfonamideHCID 1367036568.4%

Reaction Steps

A solution of 11.3 g (0.0436 mol) N-(1,1-dimethylethyl)-2-(methylthio)benzenesulfonamide in 300 ml tetrahydrofuran (THF) was treated with 60.5 ml (0.096 mol) 2M n-butyllithium in hexanes at -30° under a nitrogen atmosphere. The mixture was stirred for 1 hour at ambient temperature then recooled to -20° and treated with 8.3 g (0.0436 mol) of cuprous iodide (anhydrous). After 10 minutes at -15°, 4.9 ml (0.0438 mol) iodobenzene was added and the mixture was then heated to reflux overnight. Acetic acid (10 ml) was added after cooling the mixture to 15°, then 200 ml concentrated ammonium hydroxide plus 200 ml ethyl acetate was introduced and the mixture was stirred vigorously in the presence of air to facilitate removal of the copper salts. The aqueous phase was separated, extracted with more ethyl acetate and the combined organic extracts were washed successively with concentrated ammonium hydroxide, water and brine, then dried (MgSO4) and evaporated to an oil. The product crystallized from ether/hexanes to afford 10 g of material, m.p. 162°-165°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04764204
Source datasetuspto-grants-1988_08
ORD IDord-ec1eade7d6bd4b7d8bf0561849d4cd2f
Source noteuspto-grants-1988_08