HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971528Generated: October 26, 2026
Hydrochloric Acid → Diphenylmethyl 7-phenoxyacetamido-3-hydroxy-3-cephem-4-carboxylate
https://huagongshe.com/reaction/971528
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Diphenylmethyl alpha-[3-phenoxymethyl-7-oxo-2,6-diaza-4-thiabicyclo[3,2,0]hept-2-en-6-yl]-alpha-(2-chloro-1-hydroxyethylidene)acetate | HCID 70504488 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Diphenylmethyl 7-phenoxyacetamido-3-hydroxy-3-cephem-4-carboxylate | HCID 67789034 | — |
Reaction Steps
To an ice cooled solution of diphenylmethyl α-[3-phenoxymethyl-7-oxo-2,6-diaza-4-thiabicyclo[3,2,0]hept-2-en-6-yl]-α-(2-chloro-1-hydroxyethylidene)acetate (36 mg) in a mixture of methanol and tetrahydrofuran (1:1) (1.1 ml) is added 1N-hydrochloric acid (0.39 ml), warmed to the room temperature, and the mixture is stirred for 1.5 hours. The reaction mixture is poured into ice water, and is extracted with methylene chloride. The extract solution is washed with 5% aqueous sodium hydrogen carbonate solution and water, dried over sodium sulfate, and evaporated. Purification of the obtained residue by thin-layer chromatography using a mixture of benzene and ethyl acetate (3:2) gives diphenylmethyl 7-phenoxyacetamido-3-hydroxy-3-cephem-4-carboxylate (6 mg). m.p. 125°-126° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04160085 |
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| Source dataset | uspto-grants-1979_07 |
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| ORD ID | ord-6bb75c0510bf480f92788a31efb6ffa6 |
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| Source note | uspto-grants-1979_07 |
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