HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → t-Butyl 7alpha-bromo-3-methyl-3-cephem-4carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | t-Butyl 7alpha-amino-3-methyl-3-cephem-4-carboxylate | HCID 67657240 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | t-Butyl 7alpha-bromo-3-methyl-3-cephem-4carboxylate | HCID 67656826 | 50% |
Reaction Steps
To an ice-cooled mixture of t-butyl 7α-amino-3-methyl-3-cephem-4-carboxylate (1.3 g, 0.0048 mol), ethanol (30 ml), water (8.5 ml), hydrobromic acid (48%, 5.83 ml), sodium nitrite (0.48 g, 0.00696 mol) was added portionwise over 15 minutes and the mixture was stirred at ice-temperature (-5° C.) for 3 hours, saturated with sodium chloride, extracted with ethyl acetate (3 times). The combined ethyl acetate extract was washed with water, brine, dried and concentrated to give 800 mg (50%) of pure t-butyl 7α-bromo-3-methyl-3-cephem-4carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05264430 |
| Source dataset | uspto-grants-1993_11 |
| ORD ID | ord-8e2058d19a8645c49811053e138be1e2 |
| Source note | uspto-grants-1993_11 |