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m-Chloroperbenzoic acid → 86088-36-0

HRID 1380126
Notes
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Reaction equation

HRID 1380126 reaction equation
[C:1]1([CH2:7][CH2:8][CH2:9][CH:10]=[CH2:11])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.ClC1C=CC=C(C(OO)=[O:20])C=1>ClCCl>[C:1]1([CH2:7][CH2:8][CH2:9][CH:10]2[CH2:11][O:20]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 70297m-Chloroperbenzoic acidHCID 517892(Pent-4-en-1-yl)benzene

Product 1

HCID 1085579586088-36-0

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

5-Phenylpent-1-ene (14.2 g, 0.0973 mol) and m-chloroperbenzoic acid (16.79 g, 0.0973 mol) in dichloromethane (300 ml) was stirred at room temperature for 4 hours. The solution was washed with saturated aqueous sodium hydrogen carbonate solution and dried (MgSO4). The solvent was evaporated off under reduced pressure to give an oil which was distilled to give 2-(3-phenylpropyl)oxirane (b.p. 85° C., 0.4 mm.Hg).

Workup

  1. washThe solution was washed with saturated aqueous sodium hydrogen carbonate solution
  2. dry with materialdried (MgSO4)
  3. customThe solvent was evaporated off under reduced pressure
  4. customto give an oil which
  5. distillationwas distilled

Sources & evidence

ORD record
ord-205a8488e9cc4405b1ddfb57e7330eaa
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