Methanol → HCID 58575609、化合物

HRID 1189457ノート

反応式

HRID 1189457 の反応式
[NH2:1][C:2]1[C:11]([N+:12]([O-])=O)=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[C:4]([CH2:15][O:16][CH3:17])[CH:3]=1.[Cl-].[NH4+].O1CCCC1.CO>O>[NH2:1][C:2]1[C:11]([NH2:12])=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[C:4]([CH2:15][O:16][CH3:17])[CH:3]=1

参加物

6

反応物 4

HCID 887MethanolHCID 8028TetrahydrofuranHCID 25517Ammonium ChlorideHCID 58575185HCID 58575185、化合物

生成物 1

HCID 58575609HCID 58575609、化合物収率 105.3%

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
80 °C

実験手順

To a mixed liquid of 4.70 g of methyl 4-amino-2-(methoxymethyl)-5-nitrobenzoate, 750 mg of ammonium chloride, 47.0 mL of tetrahydrofuran, 94.0 mL of methanol, and 14.0 mL of water was added 7.65 g of reduced iron, followed by stirring at 80° C. overnight. After cooling to room temperature, the insoluble materials were filtered through celite and the filtrate was evaporated under reduced pressure to obtain 4.33 g of methyl 4,5-diamino-2-(methoxymethyl)benzoate as a brown solid.

後処理

  1. temperatureAfter cooling to room temperature
  2. filtrationthe insoluble materials were filtered through celite
  3. customthe filtrate was evaporated under reduced pressure

出典と根拠

ORDレコード
ord-eafa177f3dfd43d8a545603c8d2782e0
出典データセット
uspto-grants-2014_03
特許番号
US08674096B2

反応ノート

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