HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 70559499, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | t-Butyl 7-benzamido-3-methyl-3-cephem-4-carboxylate 1-oxide | HCID 70464442 | — |
| Catalyst | Tungsten | HCID 23964 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 70559499 | HCID 70559499 | 112.9% |
Reaction Steps
4.2 ml (30 mmoles) of triethylamine and 3.28 g (24 mmoles) of N-bromosuccinimide were sequentially added to a solution of 7.8 g (20 mmoles) of t-butyl 7-benzamido-3-methyl-3-cephem-4-carboxylate 1-oxide in 150 ml of methylene chloride under nitrogen and cooled in an ice bath and the mixture was irradiated with a 150 W tungsten lamp for 15 minutes. The dark-brown reaction mixture was washed with a dilute hydrochloric acid solution (pH 1) and then twice with 250 ml portions of water. The organic layer was dried over magnesium sulfate, filtered and evaporated to dryness to obtain 10.6 g (70% yield-purity 62%) of t-butyl 7-benzamido-2-bromo-3-methyl-3-cephem-4-carboxylate 1-oxide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04182870 |
| Source dataset | uspto-grants-1980_01 |
| ORD ID | ord-172a2682708944fbb0ea44b360c7bd74 |
| Source note | uspto-grants-1980_01 |