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Hydrochloric Acid → 4'-Chloro-3-ethylbiphen-4-ylamine

HRID 72289
ノート
印刷プレビュー

反応式

HRID 72289 の反応式
[Cl:1][C:2]1[CH:19]=[CH:18][C:5]([C:6]2[CH:11]=[C:10]([CH2:12][CH3:13])[C:9]([NH:14]C(=O)C)=[CH:8][CH:7]=2)=[CH:4][CH:3]=1.Cl>O1CCOCC1>[Cl:1][C:2]1[CH:19]=[CH:18][C:5]([C:6]2[CH:11]=[C:10]([CH2:12][CH3:13])[C:9]([NH2:14])=[CH:8][CH:7]=2)=[CH:4][CH:3]=1
参加物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 313Hydrochloric AcidHCID 59450487N-(4'-chloro-3-ethylbiphen-4-yl)acetamide

生成物 1

HCID 594504954'-Chloro-3-ethylbiphen-4-ylamine収率 97.1%

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒

実験手順

To a solution of N-(4′-chloro-3-ethylbiphen-4-yl)acetamide (18 g, 0.06 mol) in dioxane (126 ml), is added concentrated hydrochloric acid (36 ml) and the reaction mixture is heated at reflux for 2 hours. The dioxane is evaporated under reduced pressure. The residue is diluted with water, the solution made basic by addition of 2N aqueous potassium hydroxide solution and extracted with ethyl acetate (3×500 ml). The organic extracts are combined and concentrated under reduced pressure to give 4′-chloro-3-ethylbiphen-4-ylamine (13.5 g).

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. temperaturethe reaction mixture is heated
  2. temperatureat reflux for 2 hours
  3. customThe dioxane is evaporated under reduced pressure
  4. additionThe residue is diluted with water
  5. additionthe solution made basic by addition of 2N aqueous potassium hydroxide solution
  6. extractionextracted with ethyl acetate (3×500 ml)
  7. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-174230f29d8d42999a762870b73e9c18
出典データセット
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08828908B2

反応ノート

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