ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

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

HRID 2420484
ノート
印刷プレビュー

反応式

HRID 2420484 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 1 hour. The mixture is filtered and the filtrate is evaporated. The residue is suspended in water, the mixture is acidified to pH2 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. Th 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 1 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. customTh eluates are evaporated

出典と根拠

ORDレコード
ord-42444e5928b147f7ab9c160ddfcc2f5a
出典データセット
uspto-grants-1978_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04110468

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート