Furan, tetrahydro-2-(2,4-dinitrophenoxymethyl)- → 2-Amino-4-nitrophenyl tetrahydrofurfuryl ether
Reaktionsgleichung
[CH2:1]([O:7][C:8]1[CH:13]=[CH:12][C:11]([N+:14]([O-:16])=[O:15])=[CH:10][C:9]=1[N+:17]([O-])=O)[CH:2]1[O:6][CH2:5][CH2:4][CH2:3]1.S.[NH4+]>>[CH2:1]([O:7][C:8]1[CH:13]=[CH:12][C:11]([N+:14]([O-:16])=[O:15])=[CH:10][C:9]=1[NH2:17])[CH:2]1[O:6][CH2:5][CH2:4][CH2:3]1Komponenten
3
Versuchsvorschrift
2,4-Dinitrophenyl tetrahydrofurfuryl ether of the formula II is reduced with alkali metal or ammonium hydrogen sulphide or polysulphide at pH values from 5 to 11, preferably from 9 to 11, and temperatures between room temperature and the boiling point of the reaction mixture, preferably between 60° and 90° C., mainly to give 2-amino-4-nitrophenyl tetrahydrofurfuryl ether of the formula III.
Quellen und Nachweise
- ORD-Eintrag
- ord-ea24481eb4be4915a953beb7b6f5a21b
- Quelldatensatz
- uspto-grants-1989_08
- Patentnummer
- US04857070
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