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

HRID 2225320
ノート
印刷プレビュー

反応式

HRID 2225320 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-1017fb0b0be842cb8c69617f8751f694
出典データセット
uspto-grants-1994_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
USRE034722

反応ノート

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