HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354657Generated: October 30, 2026
Water → Ethyl 2-(2-tritylamino-4-thiazolyl)-2-(1-methylethoxyimino)-acetate
https://huagongshe.com/reaction/354657
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 2-(2-tritylamino-4-thiazolyl)-2-hydroxyiminoacetate | HCID 6802348 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Isopropyl iodide | HCID 6362 | — |
| Product | Ethyl 2-(2-tritylamino-4-thiazolyl)-2-(1-methylethoxyimino)-acetate | HCID 54071115 | — |
Reaction Steps
A mixture of 6.86 g of the anti isomer of ethyl 2-(2-tritylamino-4-thiazolyl)-2-hydroxyiminoacetate of Example 14, 3.51 g of potassium carbonate in 15 ml of dimethylformamide and 7.7 ml of isopropyl iodide was held under an argon atmosphere and stirring for 41/2 hours and then 250 ml of distilled water and 150 ml of ethyl acetate were added thereto with stirring. The mixture was decanted and the aqueous phase was washed with water and was extracted with ethyl acetate. The organic phase was dried, vacuum filtered and evaporated to dryness. The residue was taken up in ethanol and crystallization started after seeding. The mixture was vacuum filtered and the precipitate was rinsed with ethanol and empasted with petroleum ether to obtain 3.26 g of the anti isomer of ethyl 2-(2-tritylamino-4-thiazolyl)-2-(1-methylethoxyimino)-acetate melting at 182° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04376203 |
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| Source dataset | uspto-grants-1983_03 |
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| ORD ID | ord-425bdc43a1934a938630df4dafaf84c9 |
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| Source note | uspto-grants-1983_03 |
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