Acetonitrile → 1,3-Isobenzofurandione, 5-fluoro-
Reaction equation
[F-:1].[K+].C1OCCOC2C(=CC=CC=2)OCCOCCOC2C(=CC=CC=2)OC1.C(#N)C.[N+]([C:35]1[CH:36]=[C:37]2[C:42](=[O:43])[O:41][C:39](=[O:40])[C:38]2=[CH:44][CH:45]=1)([O-])=O>C(Cl)Cl>[F:1][C:35]1[CH:36]=[C:37]2[C:42](=[O:43])[O:41][C:39](=[O:40])[C:38]2=[CH:44][CH:45]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 82 °C
Procedure
To a reaction vessel equipped with a reflux condenser, nitrogen inlet and oil bath were introduced 2.008 grams (0.035 mol) anhydrous potassium fluoride, 0.458 gram (0.0013 mol) dibenzo-18-crown-6, and 20 ml. dry acetonitrile. This mixture was refluxed at about 82°C. for 30 minutes, and thereafter 3.011 grams (0.016 mol) 4-nitrophthalic anhydride was added and the mixture refluxed for an additional 43 hours. After cooling to room temperature, methylene chloride was added to the reaction mixture, and the latter filtered to remove solid material. Concentration of the filtrate under vacuum yielded 2 grams of 4-fluorophthalic anhydride containing a small amount of the dibenzo-18-crown-6. To remove this latter crown ether, the material was dissolved in aqueous potassium hydroxide, extracted with ethyl acetate, and acidified with hydrochloric acid to a pH 1. Extraction with ethyl acetate yield 1.195 grams (42% yield) of pure 4-fluorophthalic acid which can be dehydrated to yield 4-fluorophthalic anhydride.
Workup
- customTo a reaction vessel equipped with a reflux condenser, nitrogen inlet and oil bath
- temperaturethe mixture refluxed for an additional 43 hours
- temperatureAfter cooling to room temperature
- filtrationthe latter filtered
- customto remove solid material
Sources & evidence
- ORD record
- ord-1411352730b64c9891dce3fc8e672a08
- Source dataset
- uspto-grants-1976_05
- Patent number
- US03956321
Reaction notes
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