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2-(3,4-Dichlorophenyl)-2-methylpropanal → 3-(3,4-Dichlorophenyl)-3-methylbutan-2-ol

HRID 1627335
ノート
印刷プレビュー

反応式

HRID 1627335 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]([C:9]([CH3:13])([CH3:12])[CH:10]=[O:11])[CH:5]=[CH:6][C:7]=1[Cl:8].[CH3:14][Mg+].[Br-]>CCOCC>[Cl:1][C:2]1[CH:3]=[C:4]([C:9]([CH3:13])([CH3:12])[CH:10]([OH:11])[CH3:14])[CH:5]=[CH:6][C:7]=1[Cl:8]
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 820788952-(3,4-Dichlorophenyl)-2-methylpropanalHCID 178418689HCID 178418689、化合物

生成物 1

HCID 667400023-(3,4-Dichlorophenyl)-3-methylbutan-2-ol収率 90.7%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒2 回

反応条件

温度
0 °C

実験手順

To a solution of 2-(3,4-dichlorophenyl)-2-methylpropanal (47.13 g, 0.217 mol) in Et2O (223 mL) at 0° C. was added a 3.0M solution of MeMgBr (217 mL, 0.651 mol) in Et2O. After stirring 2 h at 0° C., the reaction mixture was warmed to room temperature over 1 h. Then the reaction mixture was cooled to 0° C., quenched with H2O (100 mL) and 3N HCl (200 mL), extracted with EtOAc and washed with brine. The organic layer was dried over Na2SO4 and concentrated to afford the crude product, which was purified by column chromatography to yield 3-(3,4-dichlorophenyl)-3-methylbutan-2-ol (45.9 g, 90%). 1H NMR (400 MHz, CDCl3) δ 7.46 (d, 1H), 7.37 (d, 1H), 7.21 (dd, 1H), 3.83 (m, 1H), 1.31 (s, 3H), 1.29 (s, 3H), 1.05 (d, 3H).

後処理

  1. temperaturethe reaction mixture was warmed to room temperature over 1 h
  2. temperatureThen the reaction mixture was cooled to 0° C.
  3. customquenched with H2O (100 mL) and 3N HCl (200 mL)
  4. extractionextracted with EtOAc
  5. washwashed with brine
  6. dry with materialThe organic layer was dried over Na2SO4
  7. concentrationconcentrated
  8. customto afford the crude product, which
  9. customwas purified by column chromatography

出典と根拠

ORDレコード
ord-0014bbb4f7ba47afb74dda9c11a0a32d
出典データセット
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08785488B2

反応ノート

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