HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 27262Erstellt: 25. Oktober 2026
Dimethylformamide → Ethyl 2-(2-tritylaminothiazol-4-yl)-2-allyloxyiminoacetate
https://huagongshe.com/reaction/27262
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Allyl bromide | HCID 7841 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Ethyl 2-(2-tritylamino-4-thiazolyl)-2-hydroxyiminoacetate | HCID 6802348 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Ethyl 2-(2-tritylaminothiazol-4-yl)-2-allyloxyiminoacetate | HCID 54525939 | 86,4% |
Reaktionsschritte
Allyl bromide (2.91 g) was added dropwise to a stirred suspension of ethyl 2-(2-tritylaminothiazol-4-yl)-2-hydroxyiminoacetate (syn isomer, 10 g), N,N-dimethylformamide (100 ml) and potassium carbonate (4.54 g) under ice cooling over 5 minutes, and stirred at the same temperature for 4 hours. After adding water (200 ml) to the resultant solution, the solution was extracted with diethyl ether twice. The extract was washed with a saturated aqueous solution of sodium chloride and dried over magnesium sulfate. The solution was concentrated in vacuo, and the residue was triturated with a solution of n-hexane and diethyl ether. The precipitates were collected by filtration to give ethyl 2-(2-tritylaminothiazol-4-yl)-2-allyloxyiminoacetate (syn isomer, 9.4 g), mp. 130° to 132° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04220761 |
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| Quelldatensatz | uspto-grants-1980_09 |
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| ORD ID | ord-2a046e2782934a18a6d5fb33db9480ed |
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| Quellennotiz | uspto-grants-1980_09 |
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