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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktAllyl bromideHCID 7841—
EduktPotassium CarbonateHCID 11430—
EduktEthyl 2-(2-tritylamino-4-thiazolyl)-2-hydroxyiminoacetateHCID 6802348—
LösungsmittelWaterHCID 962—
ProduktEthyl 2-(2-tritylaminothiazol-4-yl)-2-allyloxyiminoacetateHCID 5452593986,4%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04220761
Quelldatensatzuspto-grants-1980_09
ORD IDord-2a046e2782934a18a6d5fb33db9480ed
Quellennotizuspto-grants-1980_09