反应详情

温度

-78 °C

sec-Butyllithium (1.4M in cyclohexane, 2.78 ml) was added to dry tetrahydrofuran (10 mL) under nitrogen and the solution cooled to −78° C. N1-(2-(dimethylamino)ethyl)-N1,N2,N2-trimethylethane-1,2-diamine (0.674 g) was added slowly dropwise. A solution of tert-butyl(4-fluorophenethoxy)dimethylsilane (example 100, step a) (0.99 g) in dry tetrahydrofuran (3 mL) was then added dropwise over 5 minutes. Reaction mixture stirred for 2 hours at −78° C. DMF (2.1 ml) was added dropwise over 5 minutes and the mixture stirred at −78° C. for 1 hour followed by room temperature for 45 minutes. The reaction mixture was quenched by addition of water. Ethyl acetate (200 mL) was added and the organic washed three times with water, followed by twice with 2M HCl and then twice with water. The organic solution was washed with brine, dried over sodium sulphate, filtered and evaporated under reduced pressure. The crude product was purified by flash silica chromatography using 2% ethyl acetate in isohexane as solvent. Pure fractions were evaporated to dryness to afford the subtitled compound. Yield 0.5 g.

1. customReaction mixture
2. stirringthe mixture stirred at −78° C. for 1 hour
3. waitfollowed by room temperature for 45 minutes
4. customThe reaction mixture was quenched by addition of water
5. additionEthyl acetate (200 mL) was added
6. washthe organic washed three times with water
7. washThe organic solution was washed with brine
8. dry with materialdried over sodium sulphate
9. filtrationfiltered
10. customevaporated under reduced pressure
11. customThe crude product was purified by flash silica chromatography
12. customPure fractions were evaporated to dryness