HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butyl isocyanate → N-(Butylcarbamoyl)-3-methylthiophene-2-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butyl isocyanate | HCID 8110 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Methylthiophene-2-sulfonamide | HCID 341083 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-(Butylcarbamoyl)-3-methylthiophene-2-sulfonamide | HCID 13203354 | — |
Reaction Steps
To 150 ml of acetone and 3-methyl-2-thiophenesulfonamide was added 11 g of n-butyl isocyanate and 14 g of anhydrous potassium carbonate. After stirring at ambient temperature for 24 hours, the mixture was concentrated to 2/3 of its volume and poured into ice-water. The pH was adjusted to 3 by the addition of hydrochloric acid and the solid thus obtained was filtered, air dried and triturated with 1-chlorobutane to yield 10.6 g of N-(butylaminocarbonyl)-3-methyl-2-thiophenesulfonamide melting at 144°-146°. It showed absorption peaks by NMR (60 MC) at 2.6 δ (singlet, CH3), 1-1.8 δ (mult., C3H7), 3.42 δ (trip., N--CH2 --of butyl) and at 7.1 δ and 7.7 δ (2 doublets for CH's of thiophene) consistent for the desired structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04645529 |
| Source dataset | uspto-grants-1987_02 |
| ORD ID | ord-dc01c366dd624bb48a108c0d84c51912 |
| Source note | uspto-grants-1987_02 |