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HRID 544921생성일: 2026년 10월 23일

Hydrochloric Acid → Ethyl 2-(3-chloro-4-fluoro-phenylhydrazino)propionate

https://huagongshe.com/ko/reaction/544921

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Ethyl 2-methylacetoacetateHCID 701—
반응물3-Chloro-4-fluoroanilineHCID 9708—
반응물Potassium HydroxideHCID 14797—
반응물Sodium AcetateHCID 517045—
반응물Sodium NitriteHCID 23668193—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물Ethyl 2-(3-chloro-4-fluoro-phenylhydrazino)propionateHCID 6719734534.4%

반응 조건

온도0 °C

반응 단계

A mixture of 3-chloro-4-fluoroaniline (10.0 g) in a 6 N aqueous hydrochloric acid solution (35 ml) was cooled to 0° C., and thereto was added dropwise a solution of sodium nitrite (4.80 g) in H2O (6.3 ml). After being stirred at same temperature for 25 minutes, the mixture was added to a solution of ethyl 2-methylacetoacetate (11.0 g), potassium hydroxide (21.2 g) and sodium acetate (21.2 g) in ethyl alcohol (80 ml)-H2O (100 ml) in one portion at 0° C. The resultant mixture was stirred at same temperature for 2 hours, and extracted with diethyl ether. The organic layer was washed with water twice and brine followed by being dried over sodium sulfate. The insoluble materials were filtered off, and the filtrate was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=5:1-3:1) to give ethyl 2-(3-chloro-4-fluoro-phenylhydrazino)propionate (6.16 g) as a reddish solid. APCI-Mass m/Z 259/261 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07935674B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-0a179adff3f141c2962997c3878a5082
출처 메모uspto-grants-2011_05