反应 #632038

ord-925f4afc929f45159f2e5845d12a826e

反应方程式

NCCCP(O)O
3-aminopropylphosphonous acid
O=C([O-])O.[Na+]
sodium bicarbonate
CC(OC(=O)OC1CC(=O)NC1=O)OC(=O)C(C)C
compound ( 17 )
CC(OC(=O)OC1CC(=O)NC1=O)OC(=O)C(C)C
[(1-Isobutanoyloxyethoxy)carbonyloxy] Succinimide
CC(OC(=O)NCCCP(O)O)OC(=O)C(C)C
title compound ( 31 )
CC(OC(=O)NCCCP(O)O)OC(=O)C(C)C
3-{[1-Isobutanoyloxyethoxy]carbonylamino}propyl Phosphonous Acid

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    洗涤washed with 0.1 M aqueous potassium bisulfate (3×100 mL)
  2. 2
    其他The organic phase is separated
  3. 3
    干燥dried over anhydrous magnesium sulfate
  4. 4
    过滤filtered
  5. 5
    浓缩concentrated in vacuo

实验过程

To a solution of 3-aminopropylphosphonous acid (10 mmol) and sodium bicarbonate (20 mmol) in water (40 mL) is added a solution of compound (17) (10 mmol) in acetonitrile (20 mL) over 1 min. The reaction is stirred at ambient temperature for 16 h. The reaction mixture is diluted with diethyl ether (100 mL) and washed with 0.1 M aqueous potassium bisulfate (3×100 mL). The organic phase is separated, dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo to afford the title compound (31) as a white solid.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07935686B2uspto-grants-2011_05