Acetic Acid → HCID 11845781, compound

HRID 2216591Notes

Reaction equation

HRID 2216591 reaction equation
[N:1]([O-])=[O:2].[Na+].C(O)(=O)C.[N+:9]([C:12]1[CH:30]=[CH:29][C:15]([CH2:16][O:17][C:18]([N:20]2[CH2:25][CH2:24][NH:23][CH:22]([C:26]([OH:28])=[O:27])[CH2:21]2)=[O:19])=[CH:14][CH:13]=1)([O-:11])=[O:10]>O>[N+:9]([C:12]1[CH:13]=[CH:14][C:15]([CH2:16][O:17][C:18]([N:20]2[CH2:25][CH2:24][N:23]([N:1]=[O:2])[CH:22]([C:26]([OH:28])=[O:27])[CH2:21]2)=[O:19])=[CH:29][CH:30]=1)([O-:11])=[O:10]

Participants

5

Procedure

The H2O (300 mL) solution of NaNO2 (cont. 98.5%) (6.66 g) was added to the acetic acid (864 mL) solution of piperazine-1,3-dicarboxylic acid 1-(4-nitrobenzyl) ester (26.72 g) under a nitrogen atmosphere at 0° C. for 0.5 h and stirred for 1 h. In addition, the H2O (132 mL) solution of NaNO2 (cont. 98.5%) (2.41 g) was added to the solution at 0° C. for 0.5 h and stirred for 1 h. The solution was concentrated under reduced pressure and H2O (500 mL) was added to the residue. The solution was extracted with AcOEt (5 times) and organic layer was washed with brine. The mixture was dried over MgSO4, filtered and concentrated under reduced pressure to afford crude 4-nitrosopiperazine-1,3-dicarboxylic acid 1-(4-nitrobenzyl) ester as pale brown amorphous (27.83 g (gross), 25.77 g (net), 88.2%).

Workup

  1. stirringstirred for 1 h
  2. concentrationThe solution was concentrated under reduced pressure and H2O (500 mL)
  3. additionwas added to the residue
  4. extractionThe solution was extracted with AcOEt (5 times) and organic layer
  5. washwas washed with brine
  6. dry with materialThe mixture was dried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-1a86466340274a6db1d0b3f6a1c768cd
Source dataset
uspto-grants-2006_09
Patent number
US07112582B2

Reaction notes

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