Nitric Acid → 3H-1,2-benzodioxole
Reaction equation
C[C:2]1([C:11]2[CH:16]=[CH:15][C:14](C(F)(F)F)=[CH:13][CH:12]=2)OC2C=CC=CC=2[O:3]1.[N+]([O-])(O)=[O:22].O>ClC(Cl)C>[O:22]1[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=2[CH2:2][O:3]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 20 °C
Procedure
A solution of 2-methyl-2-[4-(trifluoromethyl)phenyl]-1,3-benzodioxole (5.6 g) in dichloroethane (15 ml) was added over 10 minutes to vigorously stirred nitric acid (50% w/v, 25 ml) keeping the temperature at 15°-20° C. by means of a cooling bath. The resulting reaction mixture was stirred for a further 1 hour at 20° C., poured into water (200 ml) and extracted with methylene chloride (3×100 ml). After drying over anhydrous sodium sulphate, the extract was evaporated under reduced pressure. The residue was purified by chromatography on silica gel using methylene chloride as eluant, affording the pure product benzodioxole as a pale yellow oil (5.3 g, 82%).
Workup
- customat 15°-20° C.
- customThe resulting reaction mixture
- extractionextracted with methylene chloride (3×100 ml)
- dry with materialAfter drying over anhydrous sodium sulphate
- customthe extract was evaporated under reduced pressure
- customThe residue was purified by chromatography on silica gel
Sources & evidence
- ORD record
- ord-7ddbf7d5a37a4876b2373b0bde4b66c9
- Source dataset
- uspto-grants-1994_10
- Patent number
- US05356924
Reaction notes
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