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Dimethylformamide → 4-Methoxybenzamide

HRID 2240203
ノート
印刷プレビュー

反応式

HRID 2240203 の反応式
C([C:8]1[CH:16]=[C:15]([O:17][CH3:18])[CH:14]=[CH:13][C:9]=1[C:10](O)=[O:11])C1C=CC=CC=1.C[N:20](C=O)C.C(Cl)(=O)C(Cl)=O>C(Cl)Cl>[CH3:18][O:17][C:15]1[CH:14]=[CH:13][C:9]([C:10]([NH2:20])=[O:11])=[CH:8][CH:16]=1
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 3

HCID 6228DimethylformamideHCID 65578Oxalyl chlorideHCID 225559782-Benzyl-4-methoxybenzoic acid

生成物 1

HCID 769594-Methoxybenzamide

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

To a solution of 2-benzyl-4-methoxybenzoic acid (14.2 g) in 600 mL CH2Cl2 was added a catalytic amount of DMF, followed by a solution of oxalyl chloride (8.7 g) in 100 mL of CH2Cl2. The reaction was stirred at room temp overnight, then concentrated and azeotroped with toluene (2×). The residue was dissolved in 700 mL CH2Cl2 and cooled to 0 C. Tert-butyl amine (13.9 g) was added, and the reaction was warmed to room temp. After 1.5 h, the reaction was quenched with 5% aqueous KHSO4. The organic solution was separated, washed once with saturated aqueous sodium bicarbonate, dried (Na2SO4) and concentrated to give 15.9 g of 2-benzyl-N-tert-butyl)-4-methoxybenzamide.

後処理

  1. concentrationconcentrated
  2. customazeotroped with toluene (2×)
  3. dissolutionThe residue was dissolved in 700 mL CH2Cl2
  4. temperaturecooled to 0 C
  5. additionTert-butyl amine (13.9 g) was added
  6. temperaturethe reaction was warmed to room temp
  7. waitAfter 1.5 h
  8. customthe reaction was quenched with 5% aqueous KHSO4
  9. customThe organic solution was separated
  10. washwashed once with saturated aqueous sodium bicarbonate
  11. dry with materialdried (Na2SO4)
  12. concentrationconcentrated

出典と根拠

ORDレコード
ord-7b726dcc643e41839b95d12f44fe52b9
出典データセット
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07723352B2

反応ノート

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