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3-(3,5-Dichlorophenyl)propionic acid → 3,5-Dichlorobenzenepropanol

HRID 480301
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HRID 480301 반응식
[H-].[H-].[H-].[H-].[Li+].[Al+3].[Cl:7][C:8]1[CH:9]=[C:10]([CH2:15][CH2:16][C:17](O)=[O:18])[CH:11]=[C:12]([Cl:14])[CH:13]=1>CCOCC>[Cl:7][C:8]1[CH:9]=[C:10]([CH2:15][CH2:16][CH2:17][OH:18])[CH:11]=[C:12]([Cl:14])[CH:13]=1
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참가 물질

4

반응물 2

HCID 8193053-(3,5-Dichlorophenyl)propionic acidHCID 21226445Aluminium lithium hydride

생성물 1

HCID 145813153,5-Dichlorobenzenepropanol수율 31.2%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

LiAlH4 (1M in Et2O, 10 mL, 10 mmol) was slowly added to a solution of 3-(3,5-dichlorophenyl)-propionic acid (2.19 g, 10 mmol) in Et2O (50 mL). The reaction was heated at reflux for 2 h. The reaction was cooled to room temperature and 2 N NaOH (1 mL) and aqueous NH4Cl (satd., 3 mL) as room temperature and 2 N NaOH (1 mL) and aqueous NH4Cl (satd., 3 mL) as over MgSO4, filtered, and concentrated. The product was purified by flash chromatography (25% EtOAc/hexanes) to afford 3-(3,5-dichlorophenyl)-propanol (640 mg). 1H NMR (400 MHz, CDCl3) δ 7.17 (m, 1H), 7.07 (m, 2H), 3.64 (m, 2H), 2.65 (t, 2H), 1.84 (m, 2H).

후처리

  1. temperatureThe reaction was heated
  2. temperatureat reflux for 2 h
  3. filtration2 N NaOH (1 mL) and aqueous NH4Cl (satd., 3 mL) as room temperature and 2 N NaOH (1 mL) and aqueous NH4Cl (satd., 3 mL) as over MgSO4, filtered
  4. concentrationconcentrated
  5. customThe product was purified by flash chromatography (25% EtOAc/hexanes)

출처 및 근거

ORD 기록
ord-543a9ff3e18a4667919b0d5517b39617
출처 데이터셋
uspto-grants-2003_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06649657B2

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