HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 7alpha-Bromo-3-methyl-3-cephem-4-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 7-Aminodeacetoxycephalosporanic acid | HCID 33498 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | 7alpha-Bromo-3-methyl-3-cephem-4-carboxylic acid | HCID 15280794 | 75.5% |
Reaction Steps
To an ice-cooled mixture of 7-ADCA (10.0 g, 0.4667 mol), ethanol (270 ml), water (83 ml) and hydrobromic acid (48%, 56.7 ml), sodium nitrite (4.67 g, 0.6769 mol) was added in small portions over 25 minutes and the mixture was stirred for 2.5 hours at ice-temperature. Ethanol was removed under reduced pressure and the residual mass was diluted with methylene chloride, washed with water. The aqueous washings were saturated with brine and re-extracted with methylene chloride. The combined organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated to give 9.8 g (75.5%) of 7α-bromo-3-methyl -3-cephem-4-carboxylic acid. This crude acid was directly used for the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05264429 |
| Source dataset | uspto-grants-1993_11 |
| ORD ID | ord-53779bcc29e147339cc0f8665c5ff7c9 |
| Source note | uspto-grants-1993_11 |