Dichloromethane → 2-Amino-3-(2,3,6-trifluorobenzyloxy)pyridine

HRID 1654913Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1654913
[NH2:1][C:2]1[C:7]([OH:8])=[CH:6][CH:5]=[CH:4][N:3]=1.ClCCl.[OH-].[Na+].[F:14][C:15]1[C:22]([F:23])=[CH:21][CH:20]=[C:19]([F:24])[C:16]=1[CH2:17]Br>CCCCCCCC[N+](CCCCCCCC)(CCCCCCCC)C.[Cl-].O>[NH2:1][C:2]1[C:7]([O:8][CH2:17][C:16]2[C:19]([F:24])=[CH:20][CH:21]=[C:22]([F:23])[C:15]=2[F:14])=[CH:6][CH:5]=[CH:4][N:3]=1

Komponenten

7

Edukt 4

HCID 6344DichloromethaneHCID 14798Sodium HydroxideHCID 281142-Amino-3-HydroxypyridineHCID 5190612,3,6-Trifluorobenzyl bromide

Produkt 1

HCID 200769692-Amino-3-(2,3,6-trifluorobenzyloxy)pyridine

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 21218Trioctylmethylammonium chlorideKatalysatorHCID 962WaterLösungsmittel

Versuchsvorschrift

A mixture of 2-amino-3-hydroxy pyridine (2.44 g, 0.022 mol), dichloromethane (20 ml) and 40% aqueous sodium hydroxide solution (20 ml) was stirred for five minutes, then 2,3,6-trifluorobenzyl bromide (5.00 g, 0.022 mol) and Adogen 464 (3 ml) were added and stirring continued for 16 hours. The mixture was diluted with water and extracted with dichloromethane. Drying and evaporation of the organic extracts, and trituration with ether gave the desired product. Yield 2.94 g (53%), m.p. 108°-110 ° C.

Aufarbeitung

  1. stirringstirring
  2. waitcontinued for 16 hours
  3. extractionextracted with dichloromethane
  4. customDrying
  5. customevaporation of the organic extracts, and trituration with ether

Quellen und Nachweise

ORD-Eintrag
ord-e93fa94ce9d04cc391c08702c8be4d00
Quelldatensatz
uspto-grants-1995_04
Patentnummer
US05409943

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