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3-(2-Methyl-1,3-dioxolan-2-yl)benzonitrile → [3-(2-Methyl-1,3-dioxolan-2-yl)phenyl]methanamine

HRID 2070993
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HRID 2070993 반응식
[H-].[H-].[H-].[H-].[Li+].[Al+3].[CH3:7][C:8]1([C:13]2[CH:14]=[C:15]([CH:18]=[CH:19][CH:20]=2)[C:16]#[N:17])[O:12][CH2:11][CH2:10][O:9]1>CCOCC>[CH3:7][C:8]1([C:13]2[CH:14]=[C:15]([CH2:16][NH2:17])[CH:18]=[CH:19][CH:20]=2)[O:9][CH2:10][CH2:11][O:12]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 105595463-(2-Methyl-1,3-dioxolan-2-yl)benzonitrileHCID 21226445Aluminium lithium hydride

생성물 1

HCID 10726441[3-(2-Methyl-1,3-dioxolan-2-yl)phenyl]methanamine수율 57.6%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

To a stirred solution of LiAlH4 (114 mg, 3.6 mmol) in ether at 0° C. was added 3-(2-methyl-1,3-dioxolan-2-yl)benzonitrile (0.57 g, 3.0 mmol). The reaction mixture was stirred for 4 h and quenched with H2O (0.2 mL), 20% NaOH (0.2 mL), brine (0.6 mL). The resulting mixture was stirred for 1 h and filtered over celite and concentrated. The residue was purified by column chromatography (10% MeOH in CHCl3) to provide (3-(2-methyl-1,3-dioxolan-2-yl)phenyl)methanamine (334 mg, 57%).

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후처리

  1. customquenched with H2O (0.2 mL), 20% NaOH (0.2 mL), brine (0.6 mL)
  2. stirringThe resulting mixture was stirred for 1 h
  3. filtrationfiltered over celite and
  4. concentrationconcentrated
  5. customThe residue was purified by column chromatography (10% MeOH in CHCl3)

출처 및 근거

ORD 기록
ord-a245248bd5c74dfc95e89de2d190d76d
출처 데이터셋
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08299267B2

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