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3-Dimethoxymethyl-4-nitro-benzoic Acid Methyl Ester → 4-Amino-3-dimethoxymethyl-benzoic Acid Methyl Ester

HRID 1788401
ノート
印刷プレビュー

反応式

HRID 1788401 の反応式
[CH3:1][O:2][C:3](=[O:18])[C:4]1[CH:9]=[CH:8][C:7]([N+:10]([O-])=O)=[C:6]([CH:13]([O:16][CH3:17])[O:14][CH3:15])[CH:5]=1>CO.[Pd]>[CH3:1][O:2][C:3](=[O:18])[C:4]1[CH:9]=[CH:8][C:7]([NH2:10])=[C:6]([CH:13]([O:14][CH3:15])[O:16][CH3:17])[CH:5]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

HCID 576030843-Dimethoxymethyl-4-nitro-benzoic Acid Methyl Ester

生成物 1

HCID 576031164-Amino-3-dimethoxymethyl-benzoic Acid Methyl Ester

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol溶媒2 回

実験手順

100 mg 10% Pd/C and 1 g Mg2SO4 were suspended in 20 mL methanol and were hydrogenated in a Parr apparatus at 30 psi for 15 minutes. The apparatus was opened, and 1.22 g (4.78 mmol) of Compound 5 dissolved in 40 mL methanol was added, followed by 2 mL TEA. The mixture was hydrogenated at 30 psi for 30 minutes, the catalyst was removed by means of filtration and the solution was evaporated to dryness. The solid material was dried over P2O5/H3PO4 overnight to give Compound 6.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. additionwas added
  2. waitThe mixture was hydrogenated at 30 psi for 30 minutes
  3. customthe catalyst was removed by means of filtration
  4. customthe solution was evaporated to dryness
  5. dry with materialThe solid material was dried over P2O5/H3PO4 overnight

出典と根拠

ORDレコード
ord-8abe8252512649bcaa209f9c32202d50
出典データセット
uspto-grants-2009_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07511145B2

反応ノート

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