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Potassium Carbonate → 2-(4-Hydroxy-2-butynylthio)indole

HRID 127513
ノート
印刷プレビュー

反応式

HRID 127513 の反応式
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][C:2]1=[S:10].C(=O)([O-])[O-].[K+].[K+].Cl[CH2:18][C:19]#[C:20][CH2:21][OH:22]>CC(C)=O>[OH:22][CH2:21][C:20]#[C:19][CH2:18][S:10][C:2]1[NH:1][C:9]2[C:4]([CH:3]=1)=[CH:5][CH:6]=[CH:7][CH:8]=2
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 11430Potassium CarbonateHCID 2027752-Butyn-1-ol, 4-chloro-HCID 30323102-Indolinethione

生成物 1

HCID 202847652-(4-Hydroxy-2-butynylthio)indole収率 110.6%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

To a solution of 2-indolinthione (7.45 g) in acetone (75 ml) is added potassium carbonate (7.60 g). After stirring, 4-chloro-2-butyn-1-ol (5.48 g) is added thereto. The mixture is stirred at room temperature for 5 hours and filtered. The filtrate is condensed to remove the acetone completely. The residue is dissolved into diethylamine (10 ml), kept at room temperature for 1 hour and evaporated to remove the diethylamine aiming to remove excessive agents. The residue is dissolved in ether (250 ml), washed with water, 2 N hydrochloric acid, water and a saturated saline solution successively, dried and evaporated to give the title compound as an oil (12.0 g).

後処理

  1. stirringThe mixture is stirred at room temperature for 5 hours
  2. filtrationfiltered
  3. customcondensed
  4. customto remove the acetone completely
  5. dissolutionThe residue is dissolved into diethylamine (10 ml)
  6. customevaporated
  7. customto remove the diethylamine aiming
  8. customto remove excessive agents
  9. dissolutionThe residue is dissolved in ether (250 ml)
  10. washwashed with water, 2 N hydrochloric acid, water
  11. customa saturated saline solution successively, dried
  12. customevaporated

出典と根拠

ORDレコード
ord-90b3b9c9d4a2437486afafb1e0eabcb7
出典データセット
uspto-grants-1981_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04256640

反応ノート

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