Reaktion #1012282

Reaktionsgleichung

(3R)-1,1,3-trimethyl-4-aminoindane

hydrogen

hydrogen

→

1,1,3-trimethyl-4-aminoindane

Lösungsmittel

2-propanol

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigeobtaining a mixture
2. 2
   SonstigeThe reaction vessel was sealed
3. 3
   workup.STIRRINGthe mixture was stirred at an internal temperature of 150° C.
4. 4
   Sonstigean internal pressure of 0.8 MPa for 7 hours to obtain a reaction mixture
5. 5
   SonstigeThe obtained reaction mixture
6. 6
   Temperaturwas cooled
7. 7
   Filtrationfiltered
8. 8
   WaschenThe obtained solid was washed with 20 parts by weight of 2-propanol
9. 9
   SonstigeThe washing liquid recovered
10. 10
    Waschenafter washing
11. 11
    Sonstigethe filtrate obtained by filtration
12. 12
    EinengenThe combined mixture was concentrated under reduced pressure

Vorschrift

Into a reaction vessel were charged 6.00 parts by weight of (3R)-1,1,3-trimethyl-4-aminoindane (optical purity of 96.5% ee), 0.81 parts by weight of 5% palladium-carbon (STD-type, manufactured by N. E. Chemcat Corporation), and 12 parts by weight of 2-propanol, thereby obtaining a mixture. The reaction vessel was sealed and the gas inside the reaction vessel was replaced with nitrogen. While stirring the mixture at room temperature, to the reaction vessel was charged hydrogen until the internal pressure of hydrogen in the reaction vessel reached 0.5 MPa. After 15 minutes, the gas in the reaction vessel was replaced with nitrogen, and the mixture was stirred at an internal temperature of 150° C. and an internal pressure of 0.8 MPa for 7 hours to obtain a reaction mixture. The obtained reaction mixture was cooled and filtered. The obtained solid was washed with 20 parts by weight of 2-propanol. The washing liquid recovered after washing and the filtrate obtained by filtration were combined. The combined mixture was concentrated under reduced pressure to obtain 5.82 parts by weight of 1,1,3-trimethyl-4-aminoindane. The obtained 1,1,3-trimethyl-4-aminoindane had an optical purity of 1.2% ee and a recovery rate of 97.0%.

Quelle