Ethyl pyruvate → Ethyl pyruvate 3-nitrophenylhydrazone

HRID 1804901

반응식

HRID 1804901 반응식
Cl.[N+:2]([C:5]1[CH:6]=[C:7]([NH:11][NH2:12])[CH:8]=[CH:9][CH:10]=1)([O-:4])=[O:3].[CH2:13]([O:15][C:16](=[O:20])[C:17](=O)[CH3:18])[CH3:14]>C(O)C>[CH2:13]([O:15][C:16](=[O:20])[C:17](=[N:12][NH:11][C:7]1[CH:8]=[CH:9][CH:10]=[C:5]([N+:2]([O-:4])=[O:3])[CH:6]=1)[CH3:18])[CH3:14]

참가 물질

4

반응물 2

HCID 12041Ethyl pyruvateHCID 54642853-Nitrophenylhydrazinium(1+) chloride

생성물 1

HCID 255590Ethyl pyruvate 3-nitrophenylhydrazone

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

(3-Nitro-phenyl)-hydrazine hydrochloride salt (B-4-a) (30.2 g, 0.16 mol) and 2-oxo-propionic acid ethyl ester (22.3 g, 0.19 mol) was dissolved in ethanol (300 mL). The mixture was stirred at room temperature for 4 h. The solvent was evaporated under reduced pressure to give 2-[(3-nitro-phenyl)-hydrazono]-propionic acid ethyl ester, which was used directly in the next step.

후처리

  1. customThe solvent was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-f0aadff933264e06898b74c375a2d48b
출처 데이터셋
uspto-grants-2013_01
특허 번호
US08354427B2

연결된 노트

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