HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorosulfonyl isocyanate → 5-Benzoyl-2-oxindole-1-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorosulfonyl isocyanate | HCID 70918 | — |
| Reactant | 5-Benzoyl-1,3-dihydro-2H-indol-2-one | HCID 13408164 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Benzoyl-2-oxindole-1-carboxamide | HCID 13647643 | — |
Reaction Steps
A mixture of 10.1 g. (42 mmole) of 5-benzoyl-2-oxindole, 4.4 ml. (51 mmole) of chlorosulfonyl isocyanate and 300 ml. of tetrahydrofuran was stirred at room temperature for 6 hours, and then the solvent was removed by evaporation in vacuo. The residue was added to 150 ml. of glacial acetic acid and 300 ml. of water and the resulting mixture was heated under reflux for 2 hours. The reaction mixture was cooled and the supernatant liquid was removed by decantation. The remaining gummy residue was triturated under acetonitrile to give a solid which was recovered by filtration and then recrystallized from a 1:1 mixture of n-propanol and acetonitrile. This gave 4.1 g. of the title compound as a solid, mp. 210°-211° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04556672 |
| Source dataset | uspto-grants-1985_12 |
| ORD ID | ord-c80f1609faa74282b2ebda8a321c5ccf |
| Source note | uspto-grants-1985_12 |