HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723588Generated: November 1, 2026
Sodium Acetate Trihydrate → HCID 131716049, compound
https://huagongshe.com/reaction/1723588
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Acetate Trihydrate | HCID 23665404 | — |
| Reactant | HCID 131716050 | HCID 131716050 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 131716049 | HCID 131716049 | — |
Reaction Steps
To a suspension of 7β-[2-cyclopropyloxyimino-2-(2-trifluoroacetamidothiazol-4-yl)acetamido]-3-(1,3,4-thiadiazol-2-yl)thiomethyl-3-cephem-4-carboxylic acid syn isomer) (1.1 g) in a mixture of water (23.5 ml) and tetrahydrofuran (2 ml) was added sodium acetate trihydrate (2.35 g) at ambient temperature. The mixture was stirred at the same temperature overnight to give a clear solution. The solution was washed with ethyl acetate and adjusted to pH 2 with 1N hydrochloric acid. The mixture was extracted with tetrahydrofuran twice. The extract was washed with saturated aqueous solution of sodium chloride, dried over magnesium sulfate and concentrated in vacuo. The residue was triturated with ethyl acetate to give 7β-[2-(2-amino- thiazol-4-yl)-2-(cyclopropyloxyimino)acetamido]-3-(1,3,4-thiadiazol-2-yl)thiomethyl-3-cephem-4-carboxylic acid (syn isomer) (780 mg) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04861769 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-1d7da91152574b909a306d67711f33e0 |
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| Source note | uspto-grants-1989_08 |
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