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Diethylene Glycol → 2-Butyl-5-chloro-1-benzofuran

HRID 1577025
ノート
印刷プレビュー

反応式

HRID 1577025 の反応式
[C:1]([C:6]1[O:7][C:8]2[CH:14]=[CH:13][C:12]([Cl:15])=[CH:11][C:9]=2[CH:10]=1)(=O)[CH2:2][CH2:3][CH3:4].NN.C(O)COCCO.[OH-].[K+]>O>[CH2:1]([C:6]1[O:7][C:8]2[CH:14]=[CH:13][C:12]([Cl:15])=[CH:11][C:9]=2[CH:10]=1)[CH2:2][CH2:3][CH3:4]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 8117Diethylene GlycolHCID 9321HydrazineHCID 14797Potassium HydroxideHCID 215104891-(5-Chloro-1-benzofuran-2-yl)butan-1-one

生成物 1

HCID 138150732-Butyl-5-chloro-1-benzofuran

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

A mixture of 31.5 g. (0.14 mol.) of 2-butyryl-5-chlorobenzofuran and 35 ml. of 98% hydrazine in 70 ml. of diethylene glycol was warmed for a few minutes on a steam bath. Then 23.3 g. of potassium hydroxide was added and the reaction mixture was refluxed for two hours. After cooling, water was added to the mixture and the resulting aqueous solution was extracted with benzene. The extract was washed with water, 10% aqueous hydrochloric acid and water, dried (MgSO4) and concentrated in vacuo to yield 2-n-butyl-5-chlorobenzofuran, b.p. 70°-75° (10-15 mm.).

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. additionA mixture of 31.5 g
  2. temperaturethe reaction mixture was refluxed for two hours
  3. temperatureAfter cooling
  4. extractionthe resulting aqueous solution was extracted with benzene
  5. washThe extract was washed with water, 10% aqueous hydrochloric acid and water
  6. dry with materialdried (MgSO4)
  7. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-3902d7157bf740c19c35fca165085d30
出典データセット
uspto-grants-1976_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03983245

反応ノート

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