Reaction #1884636
ord-24fe56c261d048c79e03d25dde504be0
Reaction equation
Reagents
Solvents
Conditions
Workup
- 1OtherAfter completion of the reaction
- 2Otherthe water in the reaction mixture was removed by distillation under reduced pressure
- 3workup.ADDITIONAcetic acid (10 mL) and ethyl acetate (20 mL) were added to the residue, which
- 4OtherThe crystals which precipitated
- 5Filtrationwere collected by filtration
Procedure
A mixed solution of methyl (2S,4S)-4-acetylthio-1-methyl-2-pyrrolidinecarboxylate (10.7 g), concentrated hydrochloric acid (14.9 g) and water (16 mL) was stirred at from 75 to 85° C. for 5 hours. After completion of the reaction, the water in the reaction mixture was removed by distillation under reduced pressure. Acetic acid (10 mL) and ethyl acetate (20 mL) were added to the residue, which was stirred at from 0 to 5° C. for 1 hour. The crystals which precipitated were collected by filtration to give the title compound (9.2 g, yield 95%). Nuclear magnetic resonance spectrum (400 MHz, CDCl3) δ(ppm): 2.11–2.20 (m, 1H), 2.97–3.05 (m, 1H), 3.02 (s, 3H), 3.56–3.68 (m, 2H), 3.80–3.88 (m, 1H), 4.35–4.41 (m, 1H).