Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 88783904 | HCID 88783904 | — |
| Solvent | Diethyl ether methanol | HCID 21864698 | — |
| Product | HCID 88784456 | HCID 88784456 | 89% |
Reaction Steps
A stirred suspension of diphenylmethyl 3-acetylthiomethyl-7β-formamidoceph-3-em-4-carboxylate (0.505 g) in methanol:ether (1:1, 3 ml.) at 0° was treated over 10 min. with phosphorus oxychloride (0.468 g.) The ice bath was removed and stirring continued for a further 20 min, when a clear solution resulted. The reaction was cooled to 0°, and a white crystalline precipitate appeared. Ether (15 ml.) was added and the precipitate filtered off, washed with ether and dried in vacuo to give diphenylmethyl 3-acetylthiomethyl-7β-aminoceph-3-em-4-carboxylate hydrochloride (0.456 g, 89%) as white microcrystals; m.p. 155°-160° (d) [α]D -91° (c 0.83 in DMSO), λmax (EtOH) 268 nm (ε 8,700), νmax. (Nujol) 1770 (β-lactam), 1720 (CO2R), 1702 cm.-1 (SCOCH3), τ (DMSO-d6) values include 2.60 (m; Ph), 3.02 (s, CHPh2), 7.66 (s, SCOCH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04209616 |
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| Source dataset | uspto-grants-1980_06 |
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| ORD ID | ord-11a53f53e1a34f1d8d1b7ed9b524bbc8 |
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| Source note | uspto-grants-1980_06 |
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