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Tetrahydrofuran → 2-(Methylthio)benzylamine

HRID 399589
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인쇄 미리보기

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HRID 399589 반응식
[CH3:1][S:2][C:3]1[CH:10]=[CH:9][CH:8]=[CH:7][C:4]=1[C:5]#[N:6].[H-].[Al+3].[Li+].[H-].[H-].[H-].C1COCC1.[OH-].[Na+]>CCOCC.O>[CH3:1][S:2][C:3]1[CH:10]=[CH:9][CH:8]=[CH:7][C:4]=1[CH2:5][NH2:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 8028TetrahydrofuranHCID 14798Sodium HydroxideHCID 1387812-(Methylthio)benzonitrileHCID 21226445Aluminium lithium hydride

생성물 1

HCID 27369812-(Methylthio)benzylamine

시약·촉매·용매 2

HCID 962Water용매2회

실험 절차

A solution of 2-(methylthio)benzonitrile (29.8 g) in dry ether (150 ml ) was added dropwise to a stirred suspension of lithium aluminium hydride (11.6 g) in dry ether (360 ml) under nitrogen. A thick gum formed which was dissolved by the addition of dry THF (100 ml). The mixture was stirred at room temperature for 2 hours, Water (12 ml) was then carefully added followed by a 15% aqueous solution of sodium hydroxide (36 ml) and more water (12 ml). The mixture, was filtered, the filtrate washed with water, dried and evaporated in vacuo. The residue was distilled in vacuo to give a colourless oil. Yield=20.9 g.

후처리

  1. customA thick gum formed which
  2. filtrationThe mixture, was filtered
  3. washthe filtrate washed with water
  4. customdried
  5. customevaporated in vacuo
  6. distillationThe residue was distilled in vacuo
  7. customto give a colourless oil

출처 및 근거

ORD 기록
ord-40c51c16553c46118715a76652942f7d
출처 데이터셋
uspto-grants-1998_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05821366

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이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
HCID 3283
Diethyl Ether
용매
2회