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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982038Generated: November 3, 2026

Hydrochloric Acid → 7-(2-Methoxyimino-3,3-ethylenedioxybutyramido)-3-cephem-4-carboxylic acid

https://huagongshe.com/reaction/1982038

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantSodium BicarbonateHCID 516892—
Reactant7-(2-Methoxyimino-3,3-ethylenedioxybutyramido)-3-hydroxycepham-4-carboxylic acidHCID 131712981—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
Product7-(2-Methoxyimino-3,3-ethylenedioxybutyramido)-3-cephem-4-carboxylic acidHCID 13171253162.9%

Reaction Steps

Trifluoroacetic anhydride (0.1 ml.) and triethylamine (0.2 ml.) were added to a solution of 7-(2-methoxyimino-3,3-ethylenedioxybutyramido)-3-hydroxycepham-4-carboxylic acid (syn isomer, 50 mg.) in dry tetrahydrofuran (5 ml.) and stirred at room temperature for 10 minutes. A sodium bicarbonate aqueous solution (2 ml.) was added to the resultant solution and heated for two minutes. Ethyl acetate and water were added to the solution, acidified with 6N hydrochloric acid and extracted with ethyl acetate. The aqueous layer was extracted with ethyl acetate. The ethyl acetate layer and extract were combined together, washed with water and a sodium chloride aqueous solution in turn and dried over magnesium sulfate. The solution was evaporated in vacuo, and the residue was pulverized with diethyl ether to give 7-(2-methoxyimino-3,3-ethylenedioxybutyramido)-3-cephem-4-carboxylic acid (syn isomer, 30 mg.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04594446
Source datasetuspto-grants-1986_06
ORD IDord-c0d834266b83463e9d1c6ccc0160fb98
Source noteuspto-grants-1986_06