HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707183Generated: October 30, 2026
Phosphorus oxychloride → HCID 70595001, compound
https://huagongshe.com/reaction/1707183
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 88784431 | HCID 88784431 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 70595001 | HCID 70595001 | — |
Reaction Steps
Phosphorus oxychloride (1.8 ml.) was added dropwise during 2 minutes to a stirred and cooled (0°) suspension of diphenylmethyl 7β-formamido-3-(5-methyl-1,3,4-thiadiazol-2-yl)thiomethylceph-3-em-4-carboxylate (4.1 g) in dry methanol. After 30 minutes the yellow solution was concentrated under reduced pressure. Ethyl acetate was added to the residue and the resulting solid was collected and washed with ether to give the title hydrochloride λmax. (EtOH) 266 nm (ε11,300), νmax. (Nujol) include 2590 (NH3+), 1778 (β-lactam) and 1710 cm.-1 (ester), τ values (DMSO-d6) include 0.50 (broad m; NH3), 2.3-2.7 (m; phenyl protons), 3.02 (s; CHPh2), 4.66+4.76 (m; C-7 H and C-6 H), 5.39+5.69 (2ds, branches of quartet, J 13 Hz; C-3 CH2S). 6.15 (singlet; C-2 CH2 ) and 7.36 (singlet; CH3).
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-847ebe8cd14748988b9f7272438219b1 |
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| Source note | uspto-grants-1980_06 |
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