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3-Chloro-2,4-pentanedione → HCID 9344223、化合物

HRID 1498946
ノート
印刷プレビュー

反応式

HRID 1498946 の反応式
[CH3:1][C:2]1[CH:10]=[C:9]([CH3:11])[CH:8]=[CH:7][C:3]=1[C:4]([NH2:6])=[S:5].Cl[CH:13]([C:17](=O)[CH3:18])[C:14](=[O:16])[CH3:15]>C(O)C>[CH3:1][C:2]1[CH:10]=[C:9]([CH3:11])[CH:8]=[CH:7][C:3]=1[C:4]1[S:5][C:13]([C:14](=[O:16])[CH3:15])=[C:17]([CH3:18])[N:6]=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 743283-Chloro-2,4-pentanedioneHCID 25176802,4-Dimethylbenzenecarbothioamide

生成物 1

HCID 9344223HCID 9344223、化合物収率 37%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒2 回

実験手順

To ethanol (20 ml), 2,4-dimethylthiobenzamide (2.00 g) and 3-chloropentane-2,4-dione (1.79 g) were added, and the mixture was stirred under heat reflux for 4 hours. After the mixture was allowed to cool to a room temperature, from the mixture ethanol was distilled off under a reduced pressure. To the resulting residue, ethyl acetate was added, and the mixture was heated and stirred. After the mixture was allowed to cool to a room temperature, the precipitate was separated by filtration, washed with ethyl acetate, and then dried under a reduced pressure to give the title compound (1.10 g, 37%).

後処理

  1. temperatureunder heat
  2. temperaturereflux for 4 hours
  3. distillationwas distilled off under a reduced pressure
  4. additionTo the resulting residue, ethyl acetate was added
  5. temperaturethe mixture was heated
  6. stirringstirred
  7. customthe precipitate was separated by filtration
  8. washwashed with ethyl acetate
  9. customdried under a reduced pressure

出典と根拠

ORDレコード
ord-532f438747f44bc58a01e1341693363c
出典データセット
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09200008B2

反応ノート

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