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Allyl bromide → (Pent-4-en-1-yl)benzene

HRID 1380125
Notes
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Reaction equation

HRID 1380125 reaction equation
[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
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 7841Allyl bromideHCID 178419670HCID 178419670, compound

Product 1

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

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent2×

Procedure

A solution of phenethyl magnesium bromide (prepared from 25 l 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).

Workup

  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

Sources & evidence

ORD record
ord-f8358a5990264efc818245dcb3d19efe
Source dataset
uspto-grants-1986_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04579862

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes