Nitric Acid → N-(2-fluoro-4-nitro-5-carboxyphenyl)-2,3-dimethylmaleic acid imide

HRID 1381831Notes

Reaction equation

HRID 1381831 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([OH:10])=[O:9])=[CH:4][C:3]=1[N:11]1[C:15](=[O:16])[C:14]([CH3:17])=[C:13]([CH3:18])[C:12]1=[O:19].[N+:20]([O-])([OH:22])=[O:21]>S(=O)(=O)(O)O>[F:1][C:2]1[CH:7]=[C:6]([N+:20]([O-:22])=[O:21])[C:5]([C:8]([OH:10])=[O:9])=[CH:4][C:3]=1[N:11]1[C:15](=[O:16])[C:14]([CH3:17])=[C:13]([CH3:18])[C:12]1=[O:19]

Participants

4

Procedure

26.3 g of N-(2-fluoro-5-carboxyphenyl)-2,3-dimethylmaleic acid imide are introduced in portions, at 5°, into 230 ml of 96% sulphuric acid. There is then added dropwise to this mixture, while stirring vigorously at the same temperature, 5 ml of 100% nitric acid. The whole is further stirred overnight at room temperature and then poured into ice. The product which precipitates is filtered with suction, washed with water, dried and recrystallised from acetonitrile. 28 g of N-(2-fluoro-5-carboxy-4-nitrophenyl)-2,3-dimethylmaleic acid imide which has a melting point of 264°-265° is thus obtained.

Workup

  1. additionThere is then added dropwise to this mixture
  2. additionpoured into ice
  3. customThe product which precipitates
  4. filtrationis filtered with suction
  5. washwashed with water
  6. customdried
  7. customrecrystallised from acetonitrile
  8. customis thus obtained

Sources & evidence

ORD record
ord-2ce17d3e64d34d5397c0b5a1557dae96
Source dataset
uspto-grants-1989_02
Patent number
US04804400

Reaction notes

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