Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 21537772 | HCID 21537772 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21537750 | HCID 21537750 | — |
Reaction Steps
To a solution of 1.5 g of 2-(N-methylacetylamino)-3-(o-fluorobenzoyl)-5-chlorothiophene in 7 ml of ethanol is added 4 ml of 6 N aqueous hydrochloric acid. The mixture is heated at 90°C for 2 hours, evaporated under reduced pressure to a residue, neutralized with aqueous ammonia, then extracted with ether. The ether extracts are washed with water, dried over sodium sulfate, when evaporated under reduced pressure to a oil, which is chromatographed on silica gel using chloroform as an eluent to give 2-(N-methylamino)-3-(o-fluorobenzoyl)-5-chlorothiophene as crystals having a melting point of 93° - 94°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US03957783 |
|---|
| Source dataset | uspto-grants-1976_05 |
|---|
| ORD ID | ord-b6d80985481d48b7b54aa26594417ef7 |
|---|
| Source note | uspto-grants-1976_05 |
|---|