2-(Methoxymethyl)-4-nitroaniline → 2-Methoxymethyl-p-phenylenediamine

HRID 1472976ノート

反応式

HRID 1472976 の反応式
[CH3:1][O:2][CH2:3][C:4]1[CH:10]=[C:9]([N+:11]([O-])=O)[CH:8]=[CH:7][C:5]=1[NH2:6].[H][H]>C(OCC)(=O)C.[Pd]>[CH3:1][O:2][CH2:3][C:4]1[CH:10]=[C:9]([NH2:11])[CH:8]=[CH:7][C:5]=1[NH2:6]

参加物

5

反応物 2

HCID 114011432-(Methoxymethyl)-4-nitroanilineHCID 178418361HCID 178418361、化合物3 回

生成物 1

HCID 97938592-Methoxymethyl-p-phenylenediamine

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 8857Ethyl Acetate溶媒

実験手順

Into a Parr hydrogenation bottle previously purged with argon, are placed a solution of 2-methoxymethyl-4-nitroaniline (5.0 g, 27.5 mmol) in ethyl acetate (50 mL) and 0.25 g of 10% palladium on carbon. The bottle is mounted on a Parr shaker and hydrogenation is carried out under 50-60 psig (64.7-74.7 psi or 446-515 kPa) of hydrogen pressure. The pressure is carefully monitored for hydrogen uptake and additional hydrogen is introduced to keep the pressure above 50 psig. The hydrogenation is carried out for 3.5 hours after which the catalyst is removed by vacuum filtration. The filtrate is concentrated to about 25 mL and toluene (25 mL) is added to precipitate the product, which is collected by vacuum filtration and dried at 60° C. under vacuum. The product yield is 4.5 g. 1H-NMR (500 MHz, DMSO-d6) δ 3.23 (s, 3H), 4.11 (s, 2H), 4.21 (s, 2H), 4.24 (s, 2H), 6.33 (dd, 1H), 6.37 (d, 1H), 6.41 (d, 1H).

後処理

  1. customInto a Parr hydrogenation bottle previously purged with argon
  2. additionis introduced
  3. customafter which the catalyst is removed by vacuum filtration
  4. concentrationThe filtrate is concentrated to about 25 mL and toluene (25 mL)
  5. additionis added
  6. customto precipitate the product, which
  7. filtrationis collected by vacuum filtration
  8. customdried at 60° C. under vacuum

出典と根拠

ORDレコード
ord-c8981a6c3f7541b999c172325e305d88
出典データセット
uspto-grants-2015_04
特許番号
US09012691B2

反応ノート

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