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Hydrochloric Acid → 3-(3-Chlorophenyl)propan-1-ol

HRID 1093353
ノート
印刷プレビュー

反応式

HRID 1093353 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]([CH2:8][CH2:9][C:10](O)=[O:11])[CH:5]=[CH:6][CH:7]=1.O1CCCC1.B.O.Cl>O1CCCC1>[Cl:1][C:2]1[CH:3]=[C:4]([CH2:8][CH2:9][CH2:10][OH:11])[CH:5]=[CH:6][CH:7]=1
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 313Hydrochloric AcidHCID 962WaterHCID 1771643-(3-Chlorophenyl)propanoic acidHCID 2723981Borane;tetrahydrofuran

生成物 1

HCID 99896673-(3-Chlorophenyl)propan-1-ol収率 75.3%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回
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

実験手順

3-(3-Chlorophenyl)propionic acid (5.00 g) was dissolved in tetrahydrofuran (100 ml), a tetrahydrofuran-borane.tetrahydrofuran solution (1 mol/l, 34.5 ml) was added dropwise to the mixture under ice-cooling, and the mixture was stirred under ice-cooling for 30 min, and further at room temperature for 15 hr. To the reaction mixture was added water, 1 mol/l aqueous hydrochloric acid solution was added, and the mixture was extracted with ethyl acetate, washed with water, saturated aqueous sodium hydrogen carbonate solution and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give the object product (3.48 g) as a colorless oil.

後処理

  1. temperaturecooling
  2. temperaturecooling for 30 min
  3. additionwas added
  4. extractionthe mixture was extracted with ethyl acetate
  5. washwashed with water, saturated aqueous sodium hydrogen carbonate solution and saturated brine
  6. dry with materialdried over anhydrous magnesium sulfate
  7. customThe solvent was evaporated under reduced pressure

出典と根拠

ORDレコード
ord-0b810d310f3c441891b36f5dec0abbd0
出典データセット
uspto-grants-2012_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08129361B2

反応ノート

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