HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1902505Generated: November 1, 2026
HCID 70524432, compound → HCID 70524350, compound
https://huagongshe.com/reaction/1902505
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 70524432 | HCID 70524432 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 70524350 | HCID 70524350 | 55.3% |
Reaction Steps
A suspension of 10% palladium carbon (16 g) in acetic acid (50 ml) was added to a solution of t-butyl 7-(2-phenylacetamido)-3-hydroxymethyl-2-cephem-4-carboxylate (9.0 g) in ethanol (300 ml.), and the mixture was subjected to catalytic reduction at 65° C. in the presence of hydrogen at 20 atm. for 9 hours. After removing the insoluble substance by filtration, the filtrate was concentrated in vacuo. The residue was dissolved in ethyl acetate (150 ml.) and adjusted to pH 7.5 with aqueous solution of sodium bicarbonate. The organic layer was separated, washed with saturated aqueous solution of sodium chloride, dried over magnesium sulfate and concentrated in vacuo. The residue was pulverized with petroleum ether and collected by filtration to give t-butyl 7-(2-phenylacetamido)-3-hydroxymethylcepham-4-carboxylate (5.0 g.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04363807 |
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| Source dataset | uspto-grants-1982_12 |
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| ORD ID | ord-c4dd77e3214b4a0b9520b4bc3f3335b9 |
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| Source note | uspto-grants-1982_12 |
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