HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 21993392, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Nitrobenzenesulfonamide | HCID 22784 | — |
| Reactant | 2-Methoxybenzoyl chloride | HCID 88969 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 21993392 | HCID 21993392 | — |
Reaction Steps
30.0 g (0.15 mol) of 4-nitrobenzenesulfonamide are treated with 30.0 g (0.3 mol) of triethylamine in 300 ml of acetonitrile and, at 50° C., treated with 27.8 g (0.16 mol) of o-anisoyl chloride, dissolved in 20 ml of acetonitrile. After 3 hours at 50° C., the mixture is stirred into 80 ml of ice-water, and the precipitate is filtered off with suction and dried. More product can be obtained by acidifying the mother liquor;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06235680B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-ff4889aa225744e0ba65cd09b2d4ac54 |
| Source note | uspto-grants-2001_05 |