Reaktion #1726670

ord-764b28f41ebf4e6b93d8e18d62a52a39

Reaktionsgleichung

O=C1CCC(=O)N1Br
N-bromosuccinimide
C=C(C)c1ccccc1
2-phenylpropene
O=C1CCC(=O)N1Br
N-bromosuccinimide
Brc1ccccc1
bromobenzene
C=C(CBr)c1ccccc1
3-bromo-2-phenylpropene
Ausbeute 46.2%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.DISSOLUTIONwas dissolved
  2. 2
    Sonstigethe precipitate was subsequently removed by filtration
  3. 3
    Waschenwashed with chloroform
  4. 4
    workup.DISTILLATIONThe filtrate was purified by distillation under reduced pressure

Vorschrift

A mixture of 2-phenylpropene (22.4 g, 190 mmoles), N-bromosuccinimide (23.7 g, 133 mmoles) and bromobenzene (76 ml) was superheated on an oil bath at 160° C. until the N-bromosuccinimide was dissolved. The reaction mixture was cooled to room temperature, and the precipitate was subsequently removed by filtration and washed with chloroform. The filtrate was purified by distillation under reduced pressure to obtain 12.1 g of 3-bromo-2-phenylpropene (b.p. 80° C. to 85° C./3 mmHg). 1H-NMR (CDCl3)δ=4.39 (s, 2H), 5.49 (s, 1H), 5.56 (s, 1H), 7.33-7.51 (m, 5H); 13C NMR (CDCl3)δ=34.2, 117.2, 126.1, 128.3, 128.5, 137.6, 144.2.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08110519B2uspto-grants-2012_02