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Dimethylformamide → 1-(N-methyl-N-phenylamino)-4-formyl naphthalene

HRID 1197940
ノート
印刷プレビュー

反応式

HRID 1197940 の反応式
P(Cl)(Cl)(Cl)=O.CN([CH:9]=[O:10])C.[CH3:11][N:12]([C:19]1[C:28]2[C:23](=[CH:24][CH:25]=[CH:26][CH:27]=2)[CH:22]=[CH:21][CH:20]=1)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.C([O-])(=O)C.[Na+]>O>[CH3:11][N:12]([C:19]1[C:28]2[C:23](=[CH:24][CH:25]=[CH:26][CH:27]=2)[C:22]([CH:9]=[O:10])=[CH:21][CH:20]=1)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=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

6

反応物 4

HCID 6228DimethylformamideHCID 24813Phosphorus oxychlorideHCID 118606N-Methyl-N-phenylnaphthalen-1-amineHCID 517045Sodium Acetate

生成物 1

HCID 200871621-(N-methyl-N-phenylamino)-4-formyl naphthalene収率 66.3%

試薬・触媒・溶媒 1

HCID 962Water
溶媒

反応条件

温度
100 °C

実験手順

Phosphorus oxychloride (POCl3, MW 153, 0.06M, 9.18 g) was added dropwise to DMF (MW 73, 0.36M, 26.3 g), maintaining the temperature at <10° C. with external cooling. 1-(N-Methyl-N-phenylamino)-naphthalene (MW 233, 0.06M, 14 g) was added and the reaction stirred at 100° C. for 3 hours. After cooling to room temperature and pouring into water (140 ml) the mixture was neutralised to pH 6 using saturated sodium acetate solution. The aqueous mixture was extracted using dichloromethane (2×50 ml), the combined extracts washed with water (3×100 ml) before drying over MgSO4. The solvent was evaporated under reduced pressure to give 10.4 g of 1-(N-methyl-N-phenylamino)-4-formyl naphthalene as an oil (66% yield).

後処理

  1. temperaturemaintaining the temperature at <10° C. with external cooling
  2. temperatureAfter cooling to room temperature
  3. extractionThe aqueous mixture was extracted
  4. washthe combined extracts washed with water (3×100 ml)
  5. dry with materialbefore drying over MgSO4
  6. customThe solvent was evaporated under reduced pressure

出典と根拠

ORDレコード
ord-711730f3360149cb8944f3fe9846685a
出典データセット
uspto-grants-1994_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05278315

反応ノート

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