N-hydroxy-2-methoxy-5-nitrobenzamide → 2-methoxy-5-amino-N-hydroxybenzamide

HRID 1096579Notes

Reaction equation

HRID 1096579 reaction equation
[OH:1][NH:2][C:3](=[O:15])[C:4]1[CH:9]=[C:8]([N+:10]([O-])=O)[CH:7]=[CH:6][C:5]=1[O:13][CH3:14]>[Pd]>[NH2:10][C:8]1[CH:7]=[CH:6][C:5]([O:13][CH3:14])=[C:4]([CH:9]=1)[C:3]([NH:2][OH:1])=[O:15]

Participants

3

Procedure

N-Hydroxy-2-methoxy-5-nitrobenzamide (approx. 47.39 mmol) was taken up in IMS (500 ml) and 10% Pd on C (50% wet) (1 g) was added. The mixture was hydrogenated at 50 psi for 1.5 hr, then filtered through celite, and the celite washed with 2M NaOH (200 ml). The MeOH was removed in vacuo and the resulting aqueous residue washed with MTBE (100 ml). The pH of the aqueous was lowered to 7 by the careful addition of concentrated HCl, and the resulting precipitated solid collected by filtration, washed with H2O, then MTBE and dried under high vacuum overnight to give 5.33 g of the title compound (62%) as a light brown solid.

Workup

  1. filtrationfiltered through celite
  2. washthe celite washed with 2M NaOH (200 ml)
  3. customThe MeOH was removed in vacuo
  4. washthe resulting aqueous residue washed with MTBE (100 ml)
  5. additionThe pH of the aqueous was lowered to 7 by the careful addition of concentrated HCl
  6. customthe resulting precipitated solid
  7. filtrationcollected by filtration
  8. washwashed with H2O
  9. dry with materialMTBE and dried under high vacuum overnight

Sources & evidence

ORD record
ord-5d8b6b74b1914a83a88709e28be22609
Source dataset
uspto-grants-2012_03
Patent number
US08138357B2

Reaction notes

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