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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 50031생성일: 2026년 10월 23일

Hydrochloric Acid → Ethyl Pyruvate 4-Chloro-3-Fluorophenylhydrazone

https://huagongshe.com/ko/reaction/50031

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참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Ethyl 2-methylacetoacetateHCID 701—
반응물Potassium AcetateHCID 517044—
반응물4-Chloro-3-fluoroanilineHCID 2736511—
반응물Sodium NitriteHCID 23668193—
용매EthanolHCID 702—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물Ethyl Pyruvate 4-Chloro-3-FluorophenylhydrazoneHCID 7311574030.3%

반응 조건

온도0 °C

반응 단계

A solution of sodium nitrite (4.76 g, 0.069 mol) in water (6.3 mL) was added dropwise to an ice cooled mixture of 4-chloro-3-fluoroaniline (J. Am. Chem. Soc., 1996, 61, 5130-5133) (10.00 g, 0.069 mol), water (167 mL) and 37% hydrochloric acid (167 mL). After 20 minutes potassium acetate (9.81 g, 0.10 mol) was added, and then a solution of ethyl 2-methylacetoacetate (9.95 g, 0.069 mol), potassium acetate (9.81 g, 0.10 mol) in methanol (67 mL) was dropped while cooling on the ice bad. Reaction was stirred at 0° C. for 3 hours, then extracted with diethyl ether. Organic layer was washed with brine and dried. Removal of the solvent furnished a red oily residue that was treated with ethanol (100 mL) and stirred at room temperature overnight. The solid which formed was filtered a recrystallized from ethanol to give 5.4 g (30%) of title compound, mp 161-163° C. (from ethanol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710068B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-fd12142649ea4bb5af36be8b36b06f39
출처 메모uspto-grants-2004_03