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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Azobisisobutyronitrile → 29610-84-2

HRID 556520
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인쇄 미리보기

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HRID 556520 반응식
[CH3:1][O:2][CH2:3][CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1.C1C(=O)N([Br:18])C(=O)C1.CC(N=NC(C#N)(C)C)(C#N)C>C(Cl)(Cl)(Cl)Cl.C(=O)(O)[O-].[Na+]>[CH3:1][O:2][CH2:3][CH:4]([Br:18])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 6547AzobisisobutyronitrileHCID 19089Methyl phenethyl etherHCID 67184N-bromobutanimide

생성물 1

HCID 1135635029610-84-2수율 84.2%

시약·촉매·용매 2

HCID 5943Carbon Tetrachloride용매HCID 516892Sodium Bicarbonate용매

실험 절차

A solution of methylphenethylether (1.0 g, 7.34 mmol), NBS (1.96 g, 11.01 mmol) and AIBN (240 mg, 1.47 mmol) in carbon tetrachloride (30 ml) was heated under reflux for 2 hours. After cooling, the reaction mixture was diluted with saturated aqueous solution of sodium bicarbonate and extracted with chloroform. The extract was washed with saturated brine, dried over magnesium sulfate and concentrated under reduced pressure to give a crude 2-methoxy-1-phenylbromoethane (1.33 g, 84%) as brown liquid.

후처리

  1. temperatureunder reflux for 2 hours
  2. temperatureAfter cooling
  3. extractionextracted with chloroform
  4. washThe extract was washed with saturated brine
  5. dry with materialdried over magnesium sulfate
  6. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-40955e6e4a9b40ae9dc5df3302624d51
출처 데이터셋
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08058280B2

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