Reaktion #977687
ord-b9120ec755604049aec9591f8510cbb9
Reaktionsgleichung
Reagenzien
Keine
Lösungsmittel
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1Sonstigethe solvent removed under reduced pressure
- 2SonstigeThe residue was partitioned between ethyl acetate and water
- 3Waschenthe organic layer washed with brine
- 4Trocknendried over magnesium sulfate
- 5SonstigeThe ethyl acetate solution was absorbed onto silica gel, which
- 6Waschenwas eluted with 10% ethyl acetate/hexane
Vorschrift
To a solution of 1,3,3-trimethylbicyclo[2.2.1]hept-2-ylamine (5 g, 26.3 mmol) in methylene chloride (20 ml) and triethylamine (4 ml) was added chloroacetyl chloride (2.1 ml, 26.4 mmol) dropwise. The resulting solution was stirred for 12 hours, then the solvent removed under reduced pressure. The residue was partitioned between ethyl acetate and water, the organic layer washed with brine, and dried over magnesium sulfate. The ethyl acetate solution was absorbed onto silica gel, which was eluted with 10% ethyl acetate/hexane, to yield 2-chloro-N-(1,3,3-trimethylbicyclo[2,2,1]hept-2-yl)acetamide as a white solid. B. Preparation of a Compound of Formula (1) in which R1 is Cyclohexyl and R2 is Phenyl