反应详情

To an iced solution of (2S,4R)-1-benzyl 2-methyl 4-(allylthio)-4-(biphenyl-4-yl)pyrrolidine-1,2-dicarboxylate (1.85 g, 3.79 mmol) in Acetonitrile (20 mL) was added Iodotrimethylsilane (0.810 mL, 5.69 mmol). The formed light brown solution was stirred at room temperature for 2 h. Cooled with ice bath, quenched with Methyl alcohol (7.68 mL, 190 mmol). The formed light brown solution was purified by prep-HPL, and the collected fractions were evaporated on speed-vac system. The yellow residue was taken up in DCM, washed with sat. Na2CO3 and brine, dried over MgSO4, filtered, and concentrated in vacuo to afford the desired product (2S,4R)-methyl 4-(allylthio)-4-(biphenyl-4-yl)pyrrolidine-2-carboxylate (664 mg, 1.878 mmol, 49.5% yield) as a viscous oil. 1H NMR (500 MHz, MeOD) δ ppm 2.96-3.09 (m, 3 H) 3.15 (d, J=14.34 Hz, 1 H) 3.84 (d, J=12.21 Hz, 1 H) 3.96 (s, 2.5 H) 4.00 (s, 0.5 H) 4.04 (d, J=11.90 Hz, 1 H) 4.77 (dd, J=10.07, 3.05 Hz, 1 H) 5.02 (d, J=9.77 Hz, 1 H) 5.09 (d, J=17.09 Hz, 1 H) 5.54-5.68 (m, 1 H) 7.38 (t, J=7.48 Hz, 1 H) 7.44-7.54 (m, 4 H) 7.66 (d, J=7.32 Hz, 2 H) 7.71 (d, J=8.55 Hz, 2 H).

1. temperatureCooled with ice bath
2. customThe formed light brown solution was purified by prep-HPL, and the collected fractions
3. customwere evaporated on speed-vac system
4. washwashed with sat. Na2CO3 and brine
5. dry with materialdried over MgSO4
6. filtrationfiltered
7. concentrationconcentrated in vacuo