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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 335384생성일: 2026년 10월 24일

Hydrochloric Acid → Ethyl 2-chloro-2-[2-(4-methoxyphenyl)hydrazono]acetate

https://huagongshe.com/ko/reaction/335384

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물P-AnisidineHCID 7732—
반응물Ethyl 2-chloroacetoacetateHCID 11858—
반응물Sodium NitriteHCID 23668193—
반응물HCID 178418247HCID 178418247—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물Ethyl 2-chloro-2-[2-(4-methoxyphenyl)hydrazono]acetateHCID 21829645—

반응 조건

온도0 °C

반응 단계

p-anisidine (31.02 g, 0.252 mol) in 100 ml of H2O is suspended in a 250 ml 4-necked flask equipped with coolant, thermometer, dropping funnel and magnetic stirrer, and cooled to 0° C. in an ice bath. 60 ml of 37% HCl is added, followed by a solution of NaNO2 (20.95 g, 0.307 mol) in 50 ml of H2O, through a dropping funnel, maintaining the temperature below 5° C. After the addition the mixture is left under stirring at between 0 and 5° C. for 1 h, and the solution obtained is added at 0° C. to a solution containing ethyl-2-chloroacetoacetate (41.65 g, 0.254 mol), AcONa (47.84 g, 0.583 mol), AcOEt (200 ml) and H2O (100 ml). The biphasic system is stirred at between 0 and 5° C. for 1 h, and then at about 25° C. for 16 h. The phases are then separated and the organic phase is washed with a saturated solution of NaHCO3 (4×80 ml), anhydrified on Na2SO4, filtered and evaporated under low pressure. The compound of formula (IV) is obtained as a solid (about 57 g), which is used for the next stage without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08884016B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-b23de9985bec45ec933dcdd633b65db0
출처 메모uspto-grants-2014_11