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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethylene Oxide | HCID 6354 | — |
| Reactant | N-(1,1-Dimethylethyl)benzenesulfonamide | HCID 314059 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(2-hydroxyethyl)-N-(1,1-dimethylethyl)benzenesulfonamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04662933 |
|---|
| Source dataset | uspto-grants-1987_05 |
|---|
| ORD ID | ord-c0a5f3abeff142799fde8ef16c5089c6 |
|---|
| Source note | uspto-grants-1987_05 |
|---|