反応 #1350725

ord-11ba500370f74c73b38fe86ed84f1c62

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他HCl (g) bubbled into the solution until saturated
  2. 2
    濃縮concentrated in vacuo

実験手順

A solution of (2R)-3-benzyloxy-2-(N-(t-butoxycarbonyl)amino)propanoic acid (23 g, 78 mmol, [α]D-4.4° (c=2, H2O)) in methanol (250 mL) was cooled to 0° C. and HCl (g) bubbled into the solution until saturated. The resulting mixture was stirred at ambient temperature for 17 hours and then concentrated in vacuo to afford 17 g (100% yield) of (2R)-3-benzyloxy-2-aminopropanoic acid methyl ester, a compound of formula (M), as a white solid; NMR (DMSO-d6) 8.7 (br s, 3), 7.4-7.3 (m, 5), 4.5 (q, 2), 4.4 (br s, 1), 3.8 (s, 2), 3.7 (s, 3) ppm.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06541476B1uspto-grants-2003_04