Water → 3-(2-Aminobenzyl)-[1,3]-oxazinan-2-one

HRID 553390Notes

Reaction equation

HRID 553390 reaction equation
[N+:1]([C:4]1[CH:17]=[CH:16][CH:15]=[CH:14][C:5]=1[CH2:6][N:7]1[CH2:12][CH2:11][CH2:10][O:9][C:8]1=[O:13])([O-])=O.[Cl-].[NH4+].O>C(O)C.[Fe]>[NH2:1][C:4]1[CH:17]=[CH:16][CH:15]=[CH:14][C:5]=1[CH2:6][N:7]1[CH2:12][CH2:11][CH2:10][O:9][C:8]1=[O:13]

Participants

6

Reactant 3

HCID 962WaterHCID 25517Ammonium ChlorideHCID 674614643-(2-Nitrobenzyl)-[1,3]-oxazinan-2-one

Product 1

HCID 619919473-(2-Aminobenzyl)-[1,3]-oxazinan-2-one

Reagents, catalysts & solvents 2

HCID 23925IronCatalystHCID 702EthanolSolvent

Procedure

3-(2-Nitrobenzyl)-[1,3]-oxazinan-2-one (0.24 g, 1.02 mmol), iron powder (0.28 g, 5.02 mmol), ammonium chloride (0.03 g, 0.56 mmol) were suspended in ethanol (10 ml) and water (5 ml) and heated to reflux for one hour. After cooling to room temperature, the reaction mixture was filtered with suction and extracted with ethyl acetate. The organic layer was washed with a saturated brine and then dried over anhydrous sodium sulfate, and 3-(2-aminobenzyl)-[1,3]-oxazinan-2-one was obtained by evaporating the solvent under reduced pressure (0.20 g).

Workup

  1. temperatureto reflux for one hour
  2. filtrationthe reaction mixture was filtered with suction
  3. extractionextracted with ethyl acetate
  4. washThe organic layer was washed with a saturated brine
  5. dry with materialdried over anhydrous sodium sulfate

Sources & evidence

ORD record
ord-f34993fa550b42b3b69348d9e2793eb3
Source dataset
uspto-grants-2011_11
Patent number
US08048825B2

Reaction notes

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