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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977897Generated: October 30, 2026

Water → 2-(2-hydroxyethyl)-N-(1,1-dimethylethyl)benzenesulfonamide

https://huagongshe.com/reaction/977897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthylene OxideHCID 6354—
ReactantN-(1,1-Dimethylethyl)benzenesulfonamideHCID 314059—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-(2-hydroxyethyl)-N-(1,1-dimethylethyl)benzenesulfonamideHCID 13822972—

Reaction Steps

A solution of N-(1,1-dimethylethyl)benzenesulfonamide (40.0 g) in 550 ml dry tetrahydrofuran was cooled to 0° and 250 ml of 1.6M n-butyllithium added dropwise at 0°. After the addition of one equivalent of base, the solution turned yellow. After stirring for 2 hours at room temperature, the resulting suspension was cooled to 0° and 13 ml of ethylene oxide added dropwise. After stirring for 3.5 hours at room temperature, the homogeneous yellow solution was poured into water. The product was extracted with ether and dried (Na2SO4). Concentration gave a yellow oil which was purified by column chromatography [400 g silica gel, ether/hexane (1:1) followed by ethyl acetate]. Pure 2-(2-hydroxyethyl)-N-(1,1-dimethylethyl)benzenesulfonamide was obtained as a colorless oil which solidified after several days; m.p. 43°-45°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04662933
Source datasetuspto-grants-1987_05
ORD IDord-c0a5f3abeff142799fde8ef16c5089c6
Source noteuspto-grants-1987_05