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Allyl iodide → HCID 23369583、化合物

HRID 1900711
ノート
印刷プレビュー

反応式

HRID 1900711 の反応式
[OH:1][C:2]1[CH:11]=[CH:10][C:9]([CH3:12])=[C:8]2[C:3]=1[CH:4]=[CH:5][C:6](=[O:13])[NH:7]2.[CH2:14](I)[CH:15]=[CH2:16].C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O>[CH2:16]([O:1][C:2]1[CH:11]=[CH:10][C:9]([CH3:12])=[C:8]2[C:3]=1[CH:4]=[CH:5][C:6](=[O:13])[NH:7]2)[CH:15]=[CH2:14]
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

5

反応物 3

HCID 11166Allyl iodideHCID 11430Potassium CarbonateHCID 23369598HCID 23369598、化合物

生成物 1

HCID 23369583HCID 23369583、化合物収率 64.1%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
50 °C

実験手順

5-Hydroxy-8-methylcarbostyril (6.35 g, 36.3 mmol), allyl iodide (6.07 g, 36.1 mmol), n-tetrabutylammonium bromide (1.16 g, 36.1 mmol) were dissolved in dimethylformamide (108 ml). To the solution, potassium carbonate (10 g, 72.5 mmol) was added, and stirred in a bath of 50° C. for 2 hours. The solvent was evaporated, and the residue, dissolved in chloroform, was washed with water. The washed material was dried and condensed. The resultant residue was purified by silica gel column chromatography (eluent; chloroform). Recrystallization (chloroform-n-hexane) yielded 4.98 g of 5-allyloxy-8-methylcarbostyril as colorless flakes (63.8%).

後処理

  1. customThe solvent was evaporated
  2. dissolutionthe residue, dissolved in chloroform
  3. washwas washed with water
  4. customThe washed material was dried
  5. customcondensed
  6. customThe resultant residue was purified by silica gel column chromatography (eluent; chloroform)
  7. customRecrystallization (chloroform-n-hexane)

出典と根拠

ORDレコード
ord-b49c8ede6e344a4d980ee7ec72cd537e
出典データセット
uspto-grants-1996_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05576324

反応ノート

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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