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Sodium Bicarbonate → N2,N2-Dimethyl-2,3-pyridinediamine

HRID 1378439
ノート
印刷プレビュー

反応式

HRID 1378439 の反応式
[CH3:1][N:2]([CH3:12])[C:3]1[C:8]([N+:9]([O-])=O)=[CH:7][CH:6]=[CH:5][N:4]=1.C([O-])(O)=O.[Na+]>CCO>[NH2:9][C:8]1[C:3]([N:2]([CH3:12])[CH3:1])=[N:4][CH:5]=[CH:6][CH:7]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 516892Sodium Bicarbonate2 回HCID 556588N,N-dimethyl-3-nitropyridin-2-amine

生成物 1

HCID 15656134N2,N2-Dimethyl-2,3-pyridinediamine収率 85.7%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
80 °C

実験手順

A stirred mixture of the product from Step 1 (1.05 g, 0.00628 mol), stannous chloride dihydrate (7.09 g, 0.03141 mol) and absolute EtOH (13.9 ml), under nitrogen, was warmed to 80° C. during 30 minutes and kept at that temperature for an additional 30 minutes. The mixture was cooled and kept at ambient temperature for 1 hour. It was then poured onto ice (200 ml), treated slowly with solid NaHCO3 (2.88 g) and adjusted to pH 8 with saturated NaHCO3. This mixture was extracted with EtOAc; the extract was washed with water, dried (Na2SO4) and concentrated to give the titled product (0.738 g), a dark oil.

後処理

  1. temperatureThe mixture was cooled
  2. waitkept at ambient temperature for 1 hour
  3. additionIt was then poured onto ice (200 ml)
  4. extractionThis mixture was extracted with EtOAc
  5. washthe extract was washed with water
  6. dry with materialdried (Na2SO4)
  7. concentrationconcentrated

出典と根拠

ORDレコード
ord-eb8caafaef8e4e6380ca0d5784a72a7b
出典データセット
uspto-grants-1997_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05668157

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート