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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 261989생성일: 2026년 10월 27일

Water → Ethyl 2-(2-tritylaminothiazol-4-yl)-2-allyloxyiminoacetate

https://huagongshe.com/reaction/261989

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Allyl iodideHCID 11166—
반응물Potassium CarbonateHCID 11430—
반응물Ethyl 2-(2-tritylamino-4-thiazolyl)-2-hydroxyiminoacetateHCID 6802348—
용매Ethyl AcetateHCID 8857—
생성물Ethyl 2-(2-tritylaminothiazol-4-yl)-2-allyloxyiminoacetateHCID 54525939—

반응 단계

A mixture of 6.86 g of the anti isomer of ethyl 2-(2-tritylamino-4-thiazolyl)-2-hydroxyiminoacetate [Step A of Example 14], 3.51 g of potassium carbonate, 15 ml of diemethylformamide and 7 ml of allyl iodide was stirred under an inert atmosphere at room temperature for 5 hours and then 250 ml of water and 150 ml of ethyl acetate were added thereto with stirring. The mixture was decanted and the aqueous phase was washed and reextracted with ethyl acetate. The extracts were dried, vacuum filtered and evaporated to dryness. The residue was taken up in ethanol and crystallizaton was started. The mixture was cooled in an ice bath with stirring for half an hour and was then vacuum filtered. The crystals were rinsed with ethanol to obtain 4.72 g of the anti isomer of ethyl 2-(2-tritylamino-4-thiazolyl)-2-(2-propenyloxyimino)-acetate. 215 mg of the product were dissolved in 2 ml of ethanol and 2 ml of methylene chloride and the mixture was filtered. The filtrate was concentrated and diluted with ethanol. Crystallization was effected in an ice bath and the mixture was vacuum filtered. The crystals were rinsed with ethanol and dried to obtain 70 mg of the pure product which melted at 90° C. (pasty) and 160° C. (pure).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04152432
출처 데이터셋uspto-grants-1979_05
ORD IDord-3ba544f444ba41b6a25e681322befac8
출처 메모uspto-grants-1979_05