HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-Butylamine → N-(Tert-butyl)-2-thiophenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | 2-Thiophenesulfonyl chloride | HCID 85518 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(Tert-butyl)-2-thiophenesulfonamide | HCID 765814 | 94% |
Reaction Steps
To a solution of t-butylamine (8.35 g, 0.114 mol) in dry tetrahydrofuran (THF) (20 mL) cooled to 0° C. was added dropwise 2-thiophenesulfonyl chloride (5.0 g, 27.4 mmol). After the addition was completed, the reaction mixture was warmed to ambient temperature and stirred overnight. The mixture was extracted with ethyl acetate (3×80 mL) and the combined extracts were washed with water, dried over molecular sieves and concentrated. The residue was chromatographed on (silica, eluting with 25% ethyl acetate-hexane) to yield 5.62 g (94%) of solid: mp 80°-82° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05240923 |
| Source dataset | uspto-grants-1993_08 |
| ORD ID | ord-aa69ae967f5a4bb793f278550b2d69d6 |
| Source note | uspto-grants-1993_08 |