HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butyl isocyanate → HCID 13489816, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butyl isocyanate | HCID 8110 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(5-Isoxazolyl)benzenesulfonamide | HCID 13489813 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | HCID 13489816 | HCID 13489816 | 79.7% |
Reaction Steps
A solution of 8.7 g of 2-(isoxazol-5-yl)benzenesulfonamide prepared in Example 5, 4.7 g of n-butyl isocyanate and 5.4 g of potassium carbonate in 125 ml of 2-butanone was refluxed for 7 hours. The resulting suspension was concentrated to dryness in vacuo. The residue was taken up in 200 ml of water and extracted once with 100 ml of ethyl ether. The aqueous layer was acidified with 2N HCl and the resulting suspension was extracted with methylene chloride. After drying the methylene chloride extract over sodium sulfate, the solvent was evaporated off under reduced pressure. The solid residue was recrystallized from acetronitrile to give 10 g of the title compound; m.p. 110°-113° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04810282 |
| Source dataset | uspto-grants-1989_03 |
| ORD ID | ord-67a2b6ee1c6142bf8e8bfb1664652da6 |
| Source note | uspto-grants-1989_03 |