Nitric Acid → 4-Dodecyl-2-nitrophenol
Reaktionsgleichung
[CH2:1]([C:13]1[CH:18]=[CH:17][C:16]([OH:19])=[CH:15][CH:14]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].[N+:20]([O-])([OH:22])=[O:21]>C(O)(=O)C>[CH2:1]([C:13]1[CH:14]=[CH:15][C:16]([OH:19])=[C:17]([N+:20]([O-:22])=[O:21])[CH:18]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]Komponenten
4
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
7.5 g of the 4-dodecylphenol obtained in (1) above was dissolved in 25 ml of acetic acid and 12.6 ml of 30% aqueous nitric acid solution was dropwise added slowly to the resulting solution, and then the resulting mixture was subjected to reaction at about 10° C. for one hour. The reaction mixture was added to 35 g of ice water and the extraction with 35 ml of diethyl ether was conducted three times. The diethyl ether layer thus obtained was washed with 35 ml of 5% aqueous NaHCO solution, and then dried with MgSO4. Subsequently, the solvent was distilled off to obtain 5.93 g of 4-dodecyl-2-nitrophenol.
Aufarbeitung
- customthe resulting mixture was subjected to reaction at about 10° C. for one hour
- extractionthe extraction with 35 ml of diethyl ether
- customThe diethyl ether layer thus obtained
- washwas washed with 35 ml of 5% aqueous NaHCO solution
- dry with materialdried with MgSO4
- distillationSubsequently, the solvent was distilled off
Quellen und Nachweise
- ORD-Eintrag
- ord-f7fa11ca5cbf4fa1a01cace47340b0d9
- Quelldatensatz
- uspto-grants-1992_04
- Patentnummer
- US05106989
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