HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256100Generated: October 30, 2026
Hydrochloric Acid → HCID 70436365, compound
https://huagongshe.com/reaction/256100
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium hydrosulfide | HCID 28015 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Propiolic acid, allyl ester (8CI) | HCID 84443 | — |
| Reactant | HCID 14535654 | HCID 14535654 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 70436365 | HCID 70436365 | 61% |
Reaction Steps
To a cooled (-10° C.) solution of 1.5 g (2 mM) of benzhydryl 7β-phenoxyacetamido-3-diphenylphosphoryloxy-3-cephem-4-carboxylate in 12 ml of N,N-dimethylformamide were added a solution of 177 mg (2.2 mM) of 70% sodium hydrosulfide in 8 ml of N,N-dimethylformamide and 310 mg (2.4 mM) of diisopropylethylamine, and the reaction mixture was stirred for 30 minutes. Subsequently, 330 mg (3 mM) of allyl propiolate was added at the same temperature, and the reaction mixture was stirred for 40 minutes. After the reaction, 50 ml of 0.5% hydrochloric acid was added, the mixture was extracted with 100 ml of ethyl acetate, and the extract was washed with a saturated aqueous sodium chloride solution (100 ml×2) and dried over anhydrous magnesium sulfate. The solvent was evaporated, and the residue was purified by silica gel column chromatography (eluent; ethyl acetate : n-hexane=2 : 3 to 1 : 1) to give 820 mg of benzhydryl 7β-phenoxyacetamido-3-[(Z)-2allyloxycarbonylvinylthio]-3-cephem-4-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04699981 |
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| Source dataset | uspto-grants-1987_10 |
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| ORD ID | ord-c2dd6548fc734343bd77b36ef5df2df4 |
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| Source note | uspto-grants-1987_10 |
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