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Methyl 3-(4-carboxy-2-nitrophenyl)propionate → 2-Oxo-1,2,3,4-tetrahydroquinoline-7-carboxylic acid

HRID 2225320
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반응식

HRID 2225320 반응식
[C:1]([C:4]1[CH:9]=[CH:8][C:7]([CH2:10][CH2:11][C:12](OC)=[O:13])=[C:6]([N+:16]([O-])=O)[CH:5]=1)([OH:3])=[O:2].CO.[OH-].[Na+]>[Pd].CO>[C:1]([C:4]1[CH:5]=[C:6]2[C:7]([CH2:10][CH2:11][C:12](=[O:13])[NH:16]2)=[CH:8][CH:9]=1)([OH:3])=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 13242991Methyl 3-(4-carboxy-2-nitrophenyl)propionateHCID 23721981Sodium hydroxide methanol

생성물 1

HCID 132430012-Oxo-1,2,3,4-tetrahydroquinoline-7-carboxylic acid

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

5 Grams of methyl 3-(4-carboxy-2nitrophenyl)propionate, 8.87 ml of 2.226N-sodium hydroxide methanol solution, 100 ml of methanol and 1 g of 5%-Pd-C (50% in water) were well mixed together and this mixture was catalytically reduced at a normal temperature under a normal pressure. Then the catalyst was removed from the reaction mixture by filtration, and the pH of the filtrate was adjusted to about pH=1 by adding concentrated hydrochloric acid. The precipitated crystals were collected by filtration and recrystallized from methanol to obtain 3.62 g of 7-carboxy-3,4-dihydrocarbostyril in the form of colorless needle-like crystals.

후처리

  1. customThen the catalyst was removed from the reaction mixture by filtration
  2. additionby adding concentrated hydrochloric acid
  3. filtrationThe precipitated crystals were collected by filtration
  4. customrecrystallized from methanol

출처 및 근거

ORD 기록
ord-1017fb0b0be842cb8c69617f8751f694
출처 데이터셋
uspto-grants-1994_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
USRE034722

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