Reaktion #1274

ord-5cabef20e3d4416cbf3328a8863028c7

Reaktionsgleichung

CC#N
acetonitrile
CS(=O)(=O)O
Methanesulfonic acid
c1ccc2c(c1)CC1OC21
Indene oxide
O
Water
N[C@@H]1c2ccccc2C[C@@H]1O
cis 1-amino-2-indanol

Lösungsmittel

Reaktionsbedingungen

Temperatur
-20°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe mixture was warmed to 25° C. and aged for 2 h
  2. 2
    Temperaturthe mixture heated at 45° C. for 5 h
  3. 3
    SonstigeThe organic phase was separated
  4. 4
    Temperaturthe aqueous phase further heated
  5. 5
    Temperaturat reflux for 4 h with concentration to approximately 200 g/L
  6. 6
    Temperaturcooled to 5° C.
  7. 7
    Filtrationfiltered
  8. 8
    Sonstigedried in vacuo

Vorschrift

Indene oxide (117 g) diluted to a total volume of 600 mL in methylene chloride was diluted with acetonitrile (600 mL) and cooled to -20° C. Methanesulfonic acid (114 mL) was then added. The mixture was warmed to 25° C. and aged for 2 h. Water (600 mL) was added and the mixture heated at 45° C. for 5 h. The organic phase was separated and the aqueous phase further heated at reflux for 4 h with concentration to approximately 200 g/L. The solution was adjusted to pH 12.5 with 50% aqueous sodium hydroxide, and then cooled to 5° C. and filtered, dried in vacuo, to provide cis 1-amino-2-indanol.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05723615uspto-grants-1998_03