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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 7-(2-Methoxyimino-3,3-ethylenedioxybutyramido)-3-hydroxycepham-4-carboxylic acid | HCID 131712981 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 7-(2-Methoxyimino-3,3-ethylenedioxybutyramido)-3-cephem-4-carboxylic acid | HCID 131712531 | 62.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04594446 |
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| Source dataset | uspto-grants-1986_06 |
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| ORD ID | ord-c0d834266b83463e9d1c6ccc0160fb98 |
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| Source note | uspto-grants-1986_06 |
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