HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → N-(Tert-butyl)-2-thiophenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | 2-Thiophenesulfonyl chloride | HCID 85518 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | N-(Tert-butyl)-2-thiophenesulfonamide | HCID 765814 | — |
Reaction Steps
Thiophene-2-sulfonyl chloride (15 g, 0.082 mol) was dissolved in CHCl3 (200 mL) under N2 atmosphere and then cooled to 0° C. tert-Butylamine (25.9 mL, 0.246 mol) dissolved in CHCl3 (50 mL) was then added dropwise to the reaction mixture. The reaction mixture was stirred for 1 h at room temperature and then at reflux for 10 min. Toluene (700 mL) was added and the organic phase was washed with water (3×50 mL), dried, and concentrated in vacuo. The sub-title product was used without further purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08357710B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-f117a88fbbf149fa85d725169f32def7 |
| Source note | uspto-grants-2013_01 |