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3-(Trifluoromethyl)aniline → Ethyl 3-oxo-3-{[3-(trifluoromethyl)phenyl]amino}propanoate

HRID 559785
ノート
印刷プレビュー

反応式

HRID 559785 の反応式
[F:1][C:2]([F:11])([F:10])[C:3]1[CH:4]=[C:5]([CH:7]=[CH:8][CH:9]=1)[NH2:6].C(N(CC)CC)C.Cl[C:20](=[O:27])[CH2:21][C:22]([O:24][CH2:25][CH3:26])=[O:23]>CC(C)=O>[O:27]=[C:20]([NH:6][C:5]1[CH:7]=[CH:8][CH:9]=[C:3]([C:2]([F:10])([F:11])[F:1])[CH:4]=1)[CH2:21][C:22]([O:24][CH2:25][CH3:26])=[O:23]
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 73753-(Trifluoromethyl)anilineHCID 8471TriethylamineHCID 118931Ethyl 3-chloro-3-oxopropionate

生成物 1

HCID 3651864Ethyl 3-oxo-3-{[3-(trifluoromethyl)phenyl]amino}propanoate収率 99%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒2 回

実験手順

To an ice-cooled solution of 3-(trifluoromethyl)aniline (64.5 g, 0.40 mol) and triethylamine (60 ml) in acetone (700 ml) was added dropwise, ethyl 3-chloro-3-oxopropanoate (63.6 g, 0.42 mol) in acetone (50 ml). After the addition (approx. 30 minutes) stirring was continued at room temperature overnight. The solvents were removed and water (1200 ml) was added. The resulting precipitate was filtered off, thoroughly washed twice with water and then dried to afford the title compound as yellow powder (109 g, 99%).

後処理

  1. additionwas added dropwise
  2. additionAfter the addition (approx. 30 minutes)
  3. customThe solvents were removed
  4. additionwater (1200 ml) was added
  5. filtrationThe resulting precipitate was filtered off
  6. washthoroughly washed twice with water
  7. customdried

出典と根拠

ORDレコード
ord-c6fa927967324d328a84e49b75ed1b6f
出典データセット
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08063073B2

反応ノート

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