HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 11287490, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Aminobenzenesulfonamide | HCID 72894 | — |
| Reactant | 4-Chlorobutyryl chloride | HCID 78370 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 11287490 | HCID 11287490 | — |
Reaction Steps
5.8 mmol of 2-aminobenzenesulfonamide are dissolved in tetrahydrofuran (THF) at room temperature. This solution is cooled on an ice bath, and 6 mmol of 4-chlorobutanoyl chloride and 6 mmol of triethylamine are successively added. The mixture is stirred for 16 hours at room temperature, filtered and evaporated. The yellow solid obtained is taken up in 40 ml of 1N sodium hydroxide and stirred at room temperature. After complete dissolution, a white precipitate appears; it is filtered off and gives the expected product after crystallization from an ethanol/water (4/1) mixture.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05536719 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-77f896765c3a4ea9a45ca0634ed37901 |
| Source note | uspto-grants-1996_07 |