Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzenesulfonyl fluoride, 3-(chlorosulfonyl)- | HCID 75603 | — |
| Reactant | HCID 20448267 | HCID 20448267 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86736898 | HCID 86736898 | 166.2% |
Reaction Steps
2'-Amino-4'-nitromethanesulfonanilide (30.4 g; 0.13 mole) was dissolved in dry tetrahydrofuran (ca. 700 ml) and then triethylamine (13.1 g; 0.13 mole) was added and the solution was chilled to 5° C. While stirring and maintaining a temperature <10° C., While stirring and maintaining a temperature <10° C., m-fluorosulfonylbenzenesulfonyl chloride (33.8 g; 0.13 mole) was added dropwise. After the addition, the reaction was kept at the ice bath temperature for one hour and then stirring continued at room temperature for an additional hour. The reaction solution was poured into ice cold water (about 2 liters) while stirring and scratching vigorously. The product was filtered and dried to yield 50.6 g (85 percent) beige solid, m.p. 204° to 209° C. A small sample (1 g) was recrystallized from ethanol (150 ml) to yield a beige solid, m.p. 224° to 226° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04204993 |
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| Source dataset | uspto-grants-1980_05 |
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| ORD ID | ord-dd262aabefff404ba0fb38bed0af86c7 |
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| Source note | uspto-grants-1980_05 |
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