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Ammonium Acetate → 1-Amino-5-(2,3-dichlorophenyl)cyclohexen-3-one

HRID 1700484
ノート
印刷プレビュー

反応式

HRID 1700484 の反応式
[Cl:1][C:2]1[C:7]([Cl:8])=[CH:6][CH:5]=[CH:4][C:3]=1[CH:9]1[CH2:14][C:13](=O)[CH2:12][C:11](=[O:16])[CH2:10]1.C([O-])(=O)C.[NH4+:21]>C(O)C>[NH2:21][C:13]1[CH2:14][CH:9]([C:3]2[CH:4]=[CH:5][CH:6]=[C:7]([Cl:8])[C:2]=2[Cl:1])[CH2:10][C:11](=[O:16])[CH:12]=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 517165Ammonium AcetateHCID 183173185-(2,3-Dichlorophenyl)cyclohexane-1,3-dione

生成物 1

HCID 183174461-Amino-5-(2,3-dichlorophenyl)cyclohexen-3-one収率 89.2%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

A mixture of 5-(2,3-dichlorophenyl)cyclohexane-1,3-dione (1.8 g) and ammonium acetate (1.7 g) in ethanol (20 ml) was refluxed for 14 hours, and the reaction solution was concentrated under reduced pressure. To the residue was added water (20 ml), and the resulting crystals were filtered. The crystals were washed with water and toluene, and dried to give 1-amino-5-(2,3-dichlorophenyl)cyclohexen-3-one (1.6 g) as pale yellow crystals.

後処理

  1. temperaturewas refluxed for 14 hours
  2. concentrationthe reaction solution was concentrated under reduced pressure
  3. additionTo the residue was added water (20 ml)
  4. filtrationthe resulting crystals were filtered
  5. washThe crystals were washed with water and toluene
  6. customdried

出典と根拠

ORDレコード
ord-75975a1469fb4bb790a33048dc41b484
出典データセット
uspto-grants-2002_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06350749B1

反応ノート

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