Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 88683891 | HCID 88683891 | — |
| Catalyst | Tungsten | HCID 23964 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 88683827 | HCID 88683827 | 28.5% |
Reaction Steps
27 g of N-bromosuccinimide were added portionwise to an ice-cold solution of 30 g of t-butyl 7-formamido-3-methyl-3-cephem-4-carboxylate-1-oxide in 1600 ml of a 1:1 mixture of acetic acid and dichloromethane under exposure to light of two tungsten lamps of 150 W over 3 hours. After a total exposure of 4 hours, the reaction mixture was then washed 3 times with water, a saturated solution of sodium bicarbonate and again with water. The organic phase was treated with activated carbon, dried over magnesium sulfate and evaporated to dryness after filtration. The residue was subjected to preparative high pressure chromatography using a 4:1 mixture of dichloromethane and acetone as eluent to obtain by evaporation to dryness of the suitable fractions 10.7 g of t-butyl 3-bromomethyl-7-formamido-3-cephem-4-carboxylate-1-oxide having the following characteristics:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04347358 |
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| Source dataset | uspto-grants-1982_08 |
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| ORD ID | ord-96ea2594d8f749ccb4046cb2fb0369c1 |
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| Source note | uspto-grants-1982_08 |
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