Potassium Carbonate → 3,4-Bis(2,2,2-trifluoroethoxy)nitrobenzene
Reaction equation
[C:1](=[O:4])([O-])[O-].[K+].[K+].FC(F)(F)S([O:12][CH2:13][C:14]([F:17])([F:16])[F:15])(=O)=O.[N+:20]([C:23]1[CH:24]=[C:25](O)[C:26](=[CH:28][CH:29]=1)O)([O-:22])=[O:21]>CC(C)=O>[F:17][C:14]([F:15])([F:16])[CH2:13][O:12][C:28]1[CH:29]=[C:23]([N+:20]([O-:22])=[O:21])[CH:24]=[CH:25][C:26]=1[O:4][CH2:1][C:14]([F:17])([F:16])[F:15]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a refluxing mixture of 12.7 g. (0.092 mole) of potassium carbonate, 21.3 g. (0.092 mole) of 2,2,2-trifluoroethyl trifluoromethanesulfonate and 62 ml. of acetone is added dropwise 6.2 g. (0.040 mole) of 4-nitrocatechol in 62 ml. of acetone over about 2.5 hours. Refluxing is continued for a total of 24 hours, then the solution is evaporated. The residue is mixed with equal volumes of water and diethyl ether. The ether layer is separated, washed with water and saturated sodium chloride solution and dried. Evaporation provides crude 3,4-bis(2,2,2-trifluoroethoxy)nitrobenzene. Chromatographic purification on a silica gel column is effected by eluting with mixtures of chloroform and hexane. Recrystallization from cyclohexane with a small amount of benzene provides solid product, m.p. 63°-65° C.
Workup
- additionTo a refluxing mixture of 12.7 g
- temperatureRefluxing
- customis continued for a total of 24 hours
- customthe solution is evaporated
- additionThe residue is mixed with equal volumes of water and diethyl ether
- customThe ether layer is separated
- washwashed with water and saturated sodium chloride solution
- customdried
- customEvaporation
Sources & evidence
- ORD record
- ord-212aba99a9fb43f4bbf7b4c6ede818b9
- Source dataset
- uspto-grants-1979_05
- Patent number
- US04154941
Reaction notes
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