HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414797Generated: October 30, 2026
Sodium Hydroxide → HCID 56637930, compound
https://huagongshe.com/reaction/414797
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 13536855 | HCID 13536855 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 56637930 | HCID 56637930 | — |
Reaction Steps
1.42 g of ethyl (Z)-2-[2-(2,2,2-trichloroethoxycarbonylamino)thiazol-4-yl]-2-[(2-pyrrolidon-3-yl)oxyimino]acetate are suspended in 30 ml of methanol, and 3 ml of 2N sodium hydroxide are added thereto with ice-cooling. The mixture is stirred at room temperature for one hour and then refluxed for 30 minutes with heating. Then, the mixture is concentrated under reduced pressure to dryness. 5 ml of water are added to the residue, and the aqueous mixture is washed with ethyl acetate. The aqueous mixture is adjusted to pH 2 to 3 with diluted hydrochloric acid, and the mixture is extracted with a mixture of ethyl acetate and tetrahydrofuran (2:1). The extract is dried and concentrated under reduced pressure to dryness. The residue is purified by silica gel chromatography (solvent, ethyl acetate:methanol=4:1). 0.4 g of (Z)-2-[(2-(2,2,2-trichloroethoxycarbonyl-amino)thiazol-4-yl]-2-[(2-pyrrolidon-3-yl)oxyimino]acetic acid is obtained. This product begins to gradually decompose at 190° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04794186 |
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| Source dataset | uspto-grants-1988_12 |
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| ORD ID | ord-d67c8e136bdd423487cfcdbd4342da01 |
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| Source note | uspto-grants-1988_12 |
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