Reaktion #1869197

ord-5389309b1db84247bd8965dc569dee38

Reaktionsgleichung

Nc1ccc2c(c1)OCCO2
2,3-dihydro-benzo[1,4]dioxin-6-ylamine
O=C1CCC(=O)N1Br
N-bromosuccinimide
Nc1cc2c(cc1Br)OCCO2
oil
Ausbeute 93.0%
Nc1cc2c(cc1Br)OCCO2
7-Bromo-2,3-dihydro-benzo[1,4]dioxin-6-ylamine
Ausbeute 93.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethen evaporated
  2. 2
    workup.DISSOLUTIONThe residue was dissolved in ether
  3. 3
    Waschenwashed with water
  4. 4
    Trocknenbrine, dried
  5. 5
    Sonstigeevaporated

Vorschrift

A solution of 2,3-dihydro-benzo[1,4]dioxin-6-ylamine (1 g, 6.6 mmol) in tetrahydrofuran (15 ml) was cooled to −78 deg C. then treated with 1 drop of concentrated sulphuric acid followed by N-bromosuccinimide (1.2 g, 6.6 mmol). The mixture was allowed to warm to room temperature over 1 hour then evaporated. The residue was dissolved in ether, washed with water then brine, dried and evaporated to afford an oil (1.4 g, 93%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07498326B2uspto-grants-2009_03