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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256100Generated: October 30, 2026

Hydrochloric Acid → HCID 70436365, compound

https://huagongshe.com/reaction/256100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrosulfideHCID 28015—
ReactantDiisopropylethylamineHCID 81531—
ReactantPropiolic acid, allyl ester (8CI)HCID 84443—
ReactantHCID 14535654HCID 14535654—
SolventDimethylformamideHCID 6228—
ProductHCID 70436365HCID 7043636561%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04699981
Source datasetuspto-grants-1987_10
ORD IDord-c2dd6548fc734343bd77b36ef5df2df4
Source noteuspto-grants-1987_10