Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 51290Erstellt: 23. Oktober 2026

Water → 2-(cyclohexylphenylamino)-N-(1,3,3-trimethylbicyclo[2.2.1]hept-2-yl)acetamide

https://huagongshe.com/de/reaction/51290

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktN-CyclohexylanilineHCID 74567—
EduktLithium HexamethyldisilazideHCID 2733832—
Edukt2-chloro-N-(1,3,3-trimethylbicyclo[2,2,1]hept-2-yl)acetamideHCID 22251091—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-(cyclohexylphenylamino)-N-(1,3,3-trimethylbicyclo[2.2.1]hept-2-yl)acetamideHCID 10133651—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of N-cyclohexylaniline (100 mg, 0.56 mmol) in tetrahydrofuran (4 ml) at −78° C. was added LiHMDS (1 ml of a 1M solution in tetrahydrofuran) dropwise. The solution was allowed to warm to 0° C., then recooled to −78° C., and a solution of 2-chloro-N-(1,3,3-trimethylbicyclo[2,2,1]hept-2-yl)acetamide (124 mg, 0.56 mmol) in tetrahydrofuran (1 ml) added dropwise. The mixture was allowed to warm to room temperature, and was stirred for 1 hour. Water was added, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, and dried over magnesium sulfate. The ethyl acetate solution was absorbed onto silica gel, which was eluted with 3% methanol/methylene chloride, to yield 2-(cyclohexylphenylamino)-N-(1,3,3-trimethylbicyclo[2.2.1]hept-2-yl)acetamide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06713650B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-426cb6d8cdc74b3997412c5c983e5829
Quellennotizuspto-grants-2004_03