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Ammonium formate → 1-N-(propan-2-yl)benzene-1,2-diamine

HRID 1521728
ノート
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反応式

HRID 1521728 の反応式
[N+:1]([C:4]1[CH:13]=[CH:12][CH:11]=[CH:10][C:5]=1[NH:6][CH:7]([CH3:9])[CH3:8])([O-])=O.C([O-])=O.[NH4+]>C(O)C.[Pd]>[CH3:9][CH:7]([NH:6][C:5]1[C:4]([NH2:1])=[CH:13][CH:12]=[CH:11][CH:10]=1)[CH3:8]
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 2723923Ammonium formateHCID 10583518N-Isopropyl-2-nitroaniline

生成物 1

HCID 105587871-N-(propan-2-yl)benzene-1,2-diamine収率 80%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 702Ethanol溶媒

実験手順

To a solution of 2-nitro-N-(propan-2-yl)aniline (828 mg, 4.6 mmol) in ethanol (10 mL) under a nitrogen atmosphere is carefully added 20% palladium on carbon (50 mg, Degussa type) followed by ammonium formate (1.4 g, 23 mmol) and the reaction is stirred for 16 h. The suspension is carefully filtered through a bed of Celite and the filter cake is rinsed with additional ethanol (10 mL). The filtrate is concentrated and the residue is partitioned between H2O and ethyl acetate. The organic layer is dried (Na2SO4) and concentrated and the residue is purified by chromatography through a short bed of silica gel using 5% methanol/CH2Cl2 affords the title compound (552 mg, 80%) as an oil.

後処理

  1. filtrationThe suspension is carefully filtered through a bed of Celite
  2. washthe filter cake is rinsed with additional ethanol (10 mL)
  3. concentrationThe filtrate is concentrated
  4. customthe residue is partitioned between H2O and ethyl acetate
  5. dry with materialThe organic layer is dried (Na2SO4)
  6. concentrationconcentrated
  7. customthe residue is purified by chromatography through a short bed of silica gel using 5% methanol/CH2Cl2

出典と根拠

ORDレコード
ord-b0a9c5ed10184b5ba39c7cb47364b683
出典データセット
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09073926B2

反応ノート

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