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{[2-(2-Chloro-6-nitro-phenyl)-ethyl]-methyl-amino}-acetic Acid Ethyl Ester → {[2-(2-chloro-6-nitro-phenyl)-ethyl]-methyl-amino}-acetic Acid

HRID 1743840
노트
인쇄 미리보기

반응식

HRID 1743840 반응식
C([O:3][C:4](=[O:20])[CH2:5][N:6]([CH2:8][CH2:9][C:10]1[C:15]([N+:16]([O-:18])=[O:17])=[CH:14][CH:13]=[CH:12][C:11]=1[Cl:19])[CH3:7])C>Br.C(#N)C>[Cl:19][C:11]1[CH:12]=[CH:13][CH:14]=[C:15]([N+:16]([O-:18])=[O:17])[C:10]=1[CH2:9][CH2:8][N:6]([CH2:5][C:4]([OH:20])=[O:3])[CH3:7]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 69549902{[2-(2-Chloro-6-nitro-phenyl)-ethyl]-methyl-amino}-acetic Acid Ethyl Ester

생성물 1

HCID 22236602{[2-(2-chloro-6-nitro-phenyl)-ethyl]-methyl-amino}-acetic Acid

시약·촉매·용매 2

HCID 260Hydrogen Bromide용매HCID 6342Acetonitrile용매

반응 조건

온도
70 °C

실험 절차

{[2-(2-chloro-6-nitro-phenyl)-ethyl]-methyl-amino}-acetic acid ethyl ester (11.0 g, 0.0365 mole) dissolved in concentrated hydrobromic acid (48 wt. % in water, 200 mL) was allowed to stir at 70° C. overnight and then reduced to a small volume in vacuo. The residue oil was taken up in acetonitrile and the solution was evaporated in vacuo. This procedure was repeated until the water was removed and a crystalline residue remained. This material was used in the next step without further purification.

후처리

  1. customthe solution was evaporated in vacuo
  2. customwas removed
  3. customThis material was used in the next step without further purification

출처 및 근거

ORD 기록
ord-d37499c39175480b8bfb307f0675b683
출처 데이터셋
uspto-grants-2006_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07012089B2

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