Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thioacetic acid | HCID 10484 | — |
| Reactant | HCID 56977568 | HCID 56977568 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 88783904 | HCID 88783904 | — |
Reaction Steps
A solution of diphenylmethyl 3-bromomethyl-7β-formamidoceph-3-em-4-carboxylate, 1β-oxide (5.0 g) in N,N-dimethylformamide (30 ml) was treated with ethanethiolic acid (4.0 ml) and triethylamine (1.4 ml) and the reaction stirred for 1.6 hr. at +19°. The yellow solution was poured into water (100 ml) and ethyl acetate (100 ml) and the resulting insoluble solid was collected, washed with ethyl acetate and dried in vacuo over phosphorus pentoxide, to give diphenylmethyl 3-acetylthiomethyl-7β-formamidoceph-3-em-4-carboxylate, 1β-oxide (2.422 g, 49%), mp 198-199° (dec.), [α]D - 60° (c 1.0, DMSO), λmax. (EtOH) 273 nm (ε 10,300), νmax. (CHBr3) 3430 (NH), 1803 (β-lactam) 1725 (CO2R), 1695, 1505 (CONH), 1042 cm.-1 (S→O) τ (DMSO-d6), 1.66 (d J 9; NH), 1.78 (s; CHO), 2.59 (m, phenyl), 3.01 (s, CHPh2), 7.68 (s; SCH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04024134 |
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| Source dataset | uspto-grants-1977_05 |
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| ORD ID | ord-5f3886a938ad4b16a19482077af9a3cf |
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| Source note | uspto-grants-1977_05 |
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