Ethyl Bromide → Ethyl 4-[N-ethyl-(6a-methyl-5,6,6a,7,8,9-hexahydro-4H-2-phenalenyl)amino]benzoate

A suspension of sodium hydride (60%, 0.013 g) in N,N-dimethylformamide (3 ml) was added with ethyl 4-[(6a-methyl-5,6,6a,7,8,9-hexahydro-4H-2-phenalenyl)amino]benzoate (0.055 g) dissolved in N,N-dimethylformamide (2 ml), and the mixture was stirred at room temperature for 15 minutes. The reaction mixture was added with bromoethane (0.025 ml), the mixture was stirred overnight at room temperature, and then added with saturated aqueous ammonium chloride, and the mixture was extracted with diethyl ether. The organic layer was washed successively with water and saturated brine, and dried over anhydrous sodium sulfate. The organic layer was concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (developing solvent: ethyl acetate:n-hexane=1:50) to obtain the title compound (0.058 g, yield: 98%).

1. stirringthe mixture was stirred overnight at room temperature
2. extractionthe mixture was extracted with diethyl ether
3. washThe organic layer was washed successively with water and saturated brine
4. dry with materialdried over anhydrous sodium sulfate
5. concentrationThe organic layer was concentrated under reduced pressure
6. customthe resulting residue was purified by silica gel column chromatography (developing solvent: ethyl acetate:n-hexane=1:50)

ORD-Eintrag

ord-c784e902999e41899198d75946dcf8cb

Quelldatensatz

uspto-grants-2012_03

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08143260B2