Reaktion #1310

ord-d35af9b12f1b47e88a643494fdc123b8

Reaktionsgleichung

O=C(OOC(=O)c1ccccc1)c1ccccc1
benzoylperoxide
CC1(C)CCCc2cc(Br)ccc21
6-bromo-1,2,3,4-tetrahydro-1,1-dimethylnaphthalene
CC1(C)CCCc2cc(Br)ccc21
Compound F
CC1(C)CCCc2cc(Br)ccc21
6-bromo-1,2,3,4-tetrahydro-1,1-dimethylnaphthalene
O=C1CCC(=O)N1Br
N-bromosuccinimide
CC1(C)CCC(Br)c2cc(Br)ccc21
title compound
CC1(C)CCC(Br)c2cc(Br)ccc21
4,6-Dibromo-1,2,3,4-tetrahydro-1,1-dimethylnaphthalene

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe mixture was refluxed for 3 hours
  2. 2
    Filtrationfiltered
  3. 3
    Waschenthe filtrate washed with water (5 ml)
  4. 4
    TrocknenThe organic phase was dried over MgSO4
  5. 5
    Einengenconcentrated in vacuo

Vorschrift

To a solution of 1.2 g (5.0 mmol) of 6-bromo-1,2,3,4-tetrahydro-1,1-dimethylnaphthalene (Compound F) in 20 ml of CCl4 was added 0.97 g (5.5 mmol) of N-bromosuccinimide followed by 20 mg (0.08 mmol ) of benzoylperoxide. The mixture was refluxed for 3 hours, filtered and the filtrate washed with water (5 ml). The organic phase was dried over MgSO4 and then concentrated in vacuo to yield the title compound as a pale yellow oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05723620uspto-grants-1998_03