Potassium Carbonate → N-[2-fluoro-5-(3-chlorallyloxycarbonyl)-4-chlorophenyl]-2,3-dimethylmaleic acid imide

HRID 1651485Notes

Reaction equation

HRID 1651485 reaction equation
[F:1][C:2]1[CH:7]=[C:6]([Cl:8])[C:5]([C:9]([OH:11])=[O:10])=[CH:4][C:3]=1[N:12]1[C:16](=[O:17])[C:15]([CH3:18])=[C:14]([CH3:19])[C:13]1=[O:20].C(=O)([O-])[O-].[K+].[K+].[Cl:27][CH:28]=[CH:29][CH2:30]Cl>CC(=O)CC>[F:1][C:2]1[CH:7]=[C:6]([Cl:8])[C:5]([C:9]([O:11][CH2:30][CH:29]=[CH:28][Cl:27])=[O:10])=[CH:4][C:3]=1[N:12]1[C:13](=[O:20])[C:14]([CH3:19])=[C:15]([CH3:18])[C:16]1=[O:17]

Participants

5

Procedure

A mixture of 3 g of N-(2-fluoro-4-chloro-5-carboxyphenyl)-2,3-dimethylmaleic acid imide, 4.5 g of potassium carbonate, 1 ml of 1,3-dichloropropene and 50 ml of 2-butanone is heated under reflux for 16 hours. The precipitate is separated off and the filtrate is concentrated by evaporation. 3.3 g of N-[2-fluoro-5-(3-chlorallyloxycarbonyl)-4-chlorophenyl]-2,3-dimethylmaleic acid imide are obtained in the form of an oil. Refractive index nD24 1.5640.

Workup

  1. temperatureis heated
  2. temperatureunder reflux for 16 hours
  3. customThe precipitate is separated off
  4. concentrationthe filtrate is concentrated by evaporation

Sources & evidence

ORD record
ord-e9f8e50400a14819bcc504f54a7b88da
Source dataset
uspto-grants-1990_05
Patent number
US04929272

Reaction notes

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