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

HRID 1627335
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HRID 1627335 반응식
[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]
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참가 물질

4

반응물 2

HCID 820788952-(3,4-Dichlorophenyl)-2-methylpropanalHCID 178418689HCID 178418689, 화합물

생성물 1

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

시약·촉매·용매 1

HCID 3283Diethyl Ether용매2회

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온도
0 °C

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-0014bbb4f7ba47afb74dda9c11a0a32d
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08785488B2

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