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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Allyl bromide → (Pent-4-en-1-yl)benzene

HRID 845481
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반응식

HRID 845481 반응식
[CH2:1]([Mg]Br)[CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[CH2:11](Br)[CH:12]=[CH2:13]>O1CCCC1>[C:3]1([CH2:2][CH2:1][CH2:13][CH:12]=[CH2:11])[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1
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참가 물질

4

반응물 2

HCID 7841Allyl bromideHCID 178419670HCID 178419670, 화합물

생성물 1

HCID 517892(Pent-4-en-1-yl)benzene

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

A solution of phenethyl magnesium bromide (prepared from 25 g, 0.135 mol of phenethyl bromide and excess magnesium turnings) in anhydrous tetrahydrofuran (50 ml) was added to a stirred solution of allyl bromide (16.34 g, 0.135 mol) in anhydrous tetrahydrofuran (150 ml) at room temperature and under an atmosphere of dry nitrogen. The mixture was stirred at room temperature for 3 hours and the solvent was then evaporated off under reduced pressure and the residue was dissolved in ethyl acetate. The solution was washed with a saturated aqueous solution of ammonium chloride and the solvent was evaporated off under reduced pressure to give an oil which was distilled to give 5-phenylpent-1-ene as a colourless oil (b.p. 40° C., 0.5 mm, Hg).

후처리

  1. customthe solvent was then evaporated off under reduced pressure
  2. dissolutionthe residue was dissolved in ethyl acetate
  3. washThe solution was washed with a saturated aqueous solution of ammonium chloride
  4. customthe solvent was evaporated off under reduced pressure
  5. customto give an oil which
  6. distillationwas distilled

출처 및 근거

ORD 기록
ord-69601bd631e64eec803b260f03b66a81
출처 데이터셋
uspto-grants-1988_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04758573

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