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2-Chlorocyclohepta-2,4,6-trien-1-one → 2-Sulfanylcyclohepta-2,4,6-trien-1-one

HRID 261864
ノート
印刷プレビュー

反応式

HRID 261864 の反応式
Cl[C:2]1[C:3](=[O:9])[CH:4]=[CH:5][CH:6]=[CH:7][CH:8]=1.[Na+].[SH-:11]>C(O)C>[SH:11][C:2]1[C:3](=[O:9])[CH:4]=[CH:5][CH:6]=[CH:7][CH:8]=1
参加物反応条件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 196912-Chlorocyclohepta-2,4,6-trien-1-oneHCID 28015Sodium hydrosulfide

生成物 1

HCID 125576902-Sulfanylcyclohepta-2,4,6-trien-1-one

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒2 回

反応条件

温度
-70 °C

実験手順

A solution of 2-chloro-2,4,6-cycloheptatrien-1-one [2.82 g, described by T. Nozoe et al., Proc. Japan Acad., 28, 483 (1952)] in ethanol (20 ml) is added dropwise to a suspension, cooled to -70° C., of sodium sulfhydrate (2.2 g) in ethanol (20 ml). The mixture is stirred at -70° C. for two hours, allowed to warm to room temperature and stirred at room temperature for one hour. The mixture is filtered and the filtrate is evaporated. The residue is suspended in water, the mixture is acidified to pH 2 with 10% hydrochloric acid and extracted with ethyl acetate. The organic extract is dried and evaporated. The residue is dissolved in benzene and subjected to chromatography on silica gel. The eluates are evaporated to give the title compound, mp 55° C.

後処理

  1. temperatureto warm to room temperature
  2. stirringstirred at room temperature for one hour
  3. filtrationThe mixture is filtered
  4. customthe filtrate is evaporated
  5. extractionextracted with ethyl acetate
  6. extractionThe organic extract
  7. customis dried
  8. customevaporated
  9. dissolutionThe residue is dissolved in benzene
  10. customThe eluates are evaporated

出典と根拠

ORDレコード
ord-93f8fc4cedcc4464a1d9ab1fa3fa1031
出典データセット
uspto-grants-1979_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04152456

反応ノート

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