HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butyl isocyanate → N-(Butylcarbamoyl)-4-methylthiophene-3-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butyl isocyanate | HCID 8110 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Methylthiophene-3-sulfonamide | HCID 566044 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | N-(Butylcarbamoyl)-4-methylthiophene-3-sulfonamide | HCID 13203330 | — |
Reaction Steps
4-Methyl-3-thiophenesulfonamide (22 g), 125 ml of methyl ethyl ketone, 16.6 g of potassium carbonate and 14.3 g of butyl isocyanate was stirred at reflux for six hours, allowed to stand overnight and then evaporated to a syrup. Water (150 ml) was added to the residue and the mixture was filtered to remove a small amount of solid. The filtrate was acidified, cooled and the resulting intermediate was filtered off. It melted at 126°-131° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04645529 |
| Source dataset | uspto-grants-1987_02 |
| ORD ID | ord-703ea3e4ba974a3ebfba4a964c71e9ee |
| Source note | uspto-grants-1987_02 |