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Methylamine → 2-Amino-4-chloro-N-methylbenzamide

HRID 1045950
ノート
印刷プレビュー

反応式

HRID 1045950 の反応式
C1N=C[N:3](C(N2C=NC=C2)=O)[CH:2]=1.[NH2:13][C:14]1[CH:22]=[C:21]([Cl:23])[CH:20]=[CH:19][C:15]=1[C:16](O)=[O:17].CN>C1COCC1>[NH2:13][C:14]1[CH:22]=[C:21]([Cl:23])[CH:20]=[CH:19][C:15]=1[C:16]([NH:3][CH3:2])=[O:17]
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 6329MethylamineHCID 666462-Amino-4-chlorobenzoic acidHCID 682631,1'-Carbonyldiimidazole

生成物 1

HCID 138538282-Amino-4-chloro-N-methylbenzamide収率 74.3%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

Carbonyl-1,1′-diimidazole (1.70 g) was added to 2-amino-4-chlorobenzoic acid (1.50 g) in THF (22.2 mL). After stirring overnight a solution of methylamine in THF (2M, 6.6 mL) was added and the reaction stirred for 3 hours. The reaction was concentrated in vacuo and the residue dissolved in EtOAc (100 mL) and saturated aqueous sodium bicarbonate solution (50 mL). The organics were then washed with saturated aqueous sodium bicarbonate solution (50 mL) and then water (2×100 mL). The organics were extracted with 1 M HCl (4×25 mL, then 2×100 mL then 50 mL), the aqueous phase basified with potassium carbonate (˜50 g) and the organics discarded. The aqueous was then extracted with EtOAc (2×50 mL). The combined organics were dried (MgSO4, 10 g) and concentrated to give 2-amino-4-chloro-N-methylbenzamide (1.2 g, 74%).

後処理

  1. additionwas added
  2. concentrationThe reaction was concentrated in vacuo
  3. dissolutionthe residue dissolved in EtOAc (100 mL)
  4. washThe organics were then washed with saturated aqueous sodium bicarbonate solution (50 mL)
  5. extractionThe organics were extracted with 1 M HCl (4×25 mL
  6. extractionThe aqueous was then extracted with EtOAc (2×50 mL)
  7. dry with materialThe combined organics were dried (MgSO4, 10 g)
  8. concentrationconcentrated

出典と根拠

ORDレコード
ord-23fc722cfcc24f598c2a0eb96ea7dfa3
出典データセット
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08569298B2

反応ノート

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