反应详情

温度

23 °C

Sodium hydride (543 mg, 22.6 mmol, 2.00 equiv) was carefully added to a solution of (2S,4R)-1-[(benzyloxy)carbonyl]4-hydroxy-2-pyrrolidinecarboxylic acid (3-1, 3.00 g, 11.3 mmol, 1 equiv) in THF (100 nL) at 0° C., and resulting mixture was stirred for 20 minutes. Iodomethane (2.11 mL, 33.9 mmol, 3.00 equiv) was added, and the mixture was warmed to 23° C. and stirred for 20 hours. The reaction mixture was then diluted with saturated sodium bicarbonate solution washed with ethyl acetate (2×100 mL). The aqueous layer was then acidified with 1 N HCl solution to pH 3 and extracted with ethyl acetate (100 mL). This organic layer was then dried over sodium sulfate and concentrated to provide (2S,4R)-1-[(benzyloxy) carbonyl]-4-methoxy-2-pyrrolidinecarboxylic acid (3-2) as a light yellow oil. 1H NMR (400 MHz, CDCl3) major rotamer: δ 7.40–7.25 (br m, 5H), 5.20 (s, 2H), 4.52 (t, 1H, J=7.4 Hz), 4.00 (m, 1H), 3.67 (dd, 1H, J=11.4, 2.8 Hz), 3.57 (dd, 1H, J=11.4, 4.6 Hz), 3.32 (s, 31), 2.34 (m, 2H).

1. customresulting mixture
2. stirringstirred for 20 hours
3. washwashed with ethyl acetate (2×100 mL)
4. extractionextracted with ethyl acetate (100 mL)
5. dry with materialThis organic layer was then dried over sodium sulfate
6. concentrationconcentrated