3,4-Dichloroaniline → N-(3,4-Dichlorophenyl)-3-phenylacrylamide

HRID 2114328ノート

反応式

HRID 2114328 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]([CH:6]=[CH:7][C:8]=1[Cl:9])[NH2:5].C(N(CC)CC)C.[C:17](Cl)(=[O:26])/[CH:18]=[CH:19]/[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>C1COCC1>[Cl:1][C:2]1[CH:3]=[C:4]([NH:5][C:17](=[O:26])/[CH:18]=[CH:19]/[C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[CH:6]=[CH:7][C:8]=1[Cl:9]

参加物

5

反応物 3

HCID 72573,4-DichloroanilineHCID 8471TriethylamineHCID 5354261Cinnamoyl Chloride

生成物 1

HCID 5403510N-(3,4-Dichlorophenyl)-3-phenylacrylamide収率 63.2%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

3,4-Dichloroaniline (5.41 g, 33.6 mmol) and triethylamine (1.5 ML) were dissolved in 160 mL of THF and treated with trans-cinnamoyl chloride (6.71 g, 40.3 mmol) with vigorous stirring at room temperature for 2 h, and then quenched with 10 mL of H2O. The reaction mixture was extracted with EtOAc (3×100 mL). The combined organics were washed with saturated solution of Na2CO3, brine, dried over MgSO4 and then concentrated in vacuo to yield the title compound as a white crystalline solid (6.2 g, 63%), MS (ES) m/e 293 [M+H]+.

後処理

  1. customquenched with 10 mL of H2O
  2. extractionThe reaction mixture was extracted with EtOAc (3×100 mL)
  3. washThe combined organics were washed with saturated solution of Na2CO3, brine
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-d6f7cf73856444c9a066960f807595e4
出典データセット
uspto-grants-2008_10
特許番号
US07432258B2

反応ノート

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