HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 7-Benzoylamino-3-chloromethyl-3-cephem-4-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Benzhydryl 7-benzoylamino-3-chloromethyl-3-cephem-4-carboxylate | HCID 67834587 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Anisole | HCID 7519 | — |
| Product | 7-Benzoylamino-3-chloromethyl-3-cephem-4-carboxylic acid | HCID 67834677 | — |
Reaction Steps
To a solution of benzhydryl 7-benzoylamino-3-chloromethyl-3-cephem-4-carboxylate (20 g) in a mixture of dichloromethane (40 ml) and anisole (10 ml) was added trifluoroacetic acid (20 ml) under cooling. After being stirred for two hours at -3°~0° C., the mixture was added dropwise to a mixture of diisopropyl ether (400 ml) and n-hexan (800 ml) at 5° C. The stirring was continued for 15 minutes at the same temperature. The resulting powder was collected by filtration, washed with n-hexan and dried over phosphorus pentoxide to give 7-benzoylamino-3-chloromethyl-3-cephem-4-carboxylic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04868174 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-0b2e1cfb68a548bfae26c0ea761ab83b |
| Source note | uspto-grants-1989_09 |