反応 #576375

ord-960ba03bebcf4f2e8607bef30d6751b9

反応方程式

CC(C)(C)OC(=O)N[C@H](COCc1ccccc1)C(=O)O
(2R)-3-benzyloxy-2-(N-(t-butoxycarbonyl)amino)propanoic acid
CO
methanol
COC(=O)[C@H](N)COCc1ccccc1
(2R)-3-benzyloxy-2-aminopropanoic acid methyl ester
収率 100.0%

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: US06977258B2uspto-grants-2005_12