HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27965Generated: October 29, 2026
Ethanol → Sodium 3-acetoxymethyl-7-[2-(2-amino-4-thiazolyl)-2-methoxyimino-acetamido]-ceph-3-eme-4-carboxylate
https://huagongshe.com/reaction/27965
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 3-Acetoxymethyl 7-[2-(2-amino-4-thiazolyl)-2-methoxyimino-acetamido]-ceph-3-eme-4-carboxylic acid | HCID 131711503 | — |
| Solvent | Water | HCID 962 | — |
| Product | Sodium 3-acetoxymethyl-7-[2-(2-amino-4-thiazolyl)-2-methoxyimino-acetamido]-ceph-3-eme-4-carboxylate | HCID 131711736 | — |
Reaction Steps
A solution of 6 g of sodium acetate in 20 ml of water was added with stirring at 20° C. to 50 ml of 98% ethanol and with continued stirring 25 g of an ethanol solvate of the syn isomer of 3-acetoxymethyl-7-[2-(2-amino-4-thiazolyl)-2-methoxyimino-acetamido]-ceph-3-eme-4-carboxylic acid were added thereto. After dissolution occured, the solution was cooled to 0° C. and 50 ml of 98% ethanol were added thereto dropwise with stirring. Activated carbon was added to the solution which was then filtered and the filtrate was heated to 20° C. Crystallization spontaneously occured shortly thereafter and filtration by aspiration was effected at room temperature 16 hours later. The recovered product was washed with a 1-7 water-ethanol mixture, with ethanol and then with ether to obtain colorless crystals of the D form of the syn isomer of sodium 3-acetoxymethyl-7-[2-(2-amino-4-thiazolyl)-2-methoxyimino-acetamido]-ceph-3-eme-4 -carboxylate which after drying under reduced pressure contained 4.8% of water (by Fischer). The spectrum of X-ray diffraction and the infrared spectrum in nujol confirmed the D form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04224371 |
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| Source dataset | uspto-grants-1980_09 |
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| ORD ID | ord-9341e2414a574b8db0e08b4d43382356 |
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| Source note | uspto-grants-1980_09 |
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