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Water → [4-(1,3-Dioxolan-2-yl)phenyl]methanamine

HRID 2080121
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HRID 2080121 반응식
[O:1]1[CH2:5][CH2:4][O:3][CH:2]1[C:6]1[CH:13]=[CH:12][C:9]([C:10]#[N:11])=[CH:8][CH:7]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-].O.[OH-].[Na+]>O1CCCC1>[O:1]1[CH2:5][CH2:4][O:3][CH:2]1[C:6]1[CH:7]=[CH:8][C:9]([CH2:10][NH2:11])=[CH:12][CH:13]=1
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참가 물질

6

반응물 4

HCID 962Water2회HCID 14798Sodium HydroxideHCID 27784284-(1,3-Dioxolan-2-yl)benzonitrileHCID 21226445Aluminium lithium hydride

생성물 1

HCID 10559254[4-(1,3-Dioxolan-2-yl)phenyl]methanamine

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매
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실험 절차

4-[1,3]Dioxolan-2-yl-benzonitrile described in Preparation Example 119 (3.78 g, 21.6 mmol) was dissolved in tetrahydrofuran (76 mL), lithium aluminum hydride (4.09 g, 108 mmol) was added at 0° C., and the solution was stirred overnight at room temperature. Water (4.09 mL), an aqueous solution of 5N sodium hydroxide (4.09 mL) and water (12.3 mL) were sequentially added to the reaction solution. The reaction solution was filtered through Celite pad, then, the filtrate was evaporated in vacuo, and the title compound (3.92 g, quantitatively) was obtained as a pale yellow oil.

후처리

  1. filtrationThe reaction solution was filtered through Celite pad
  2. customthe filtrate was evaporated in vacuo

출처 및 근거

ORD 기록
ord-7ad26db0d3544d589d2ea46555e0d17c
출처 데이터셋
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07932272B2

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