反应详情

To a solution of 0.31 mL (3.6 mmol) of oxalyl chloride in 20 mL of CH2Cl2 at −78° C. was added 0.51 mL (7.2 mmol) of DMSO and the reaction mixture was stirred. After 10 min., a solution of 0.49 g (1.8 mmol) of 1-benzyl-3-(RS)-hydroxymethyl-4-(SR)-(3-thienyl)pyrrolidine in 20 mL of CH2Cl2 was then added. After stirring for 10 min. at −78° C., the reaction was allowed to warm to rt. The reaction mixture was poured into ether and extracted twice with sat'd NaHCO3 solution and once with sat'd NaCl solution. The organic fraction was dried over Na2SO4, filtered and the filtrate was concentrated to give 0.49 g of the title compound. 1H NMR (CDCl3) δ9.75 (d, 1H, J=2.1 Hz), 7.27-7.36 (m, 6H), 7.03-7.07 (m, 2H), 3.78 (q, 1H, J=6.8 Hz), 3.72 (d, 1H, J=13.1 Hz), 3.68 (d, 1H, J=12.8 Hz).

1. stirringAfter stirring for 10 min. at −78° C.
2. extractionextracted twice with sat'd NaHCO3 solution and once with sat'd NaCl solution
3. dry with materialThe organic fraction was dried over Na2SO4
4. filtrationfiltered
5. concentrationthe filtrate was concentrated