2,5-Dimethoxytetrahydrofuran → 1-[(2,4-Difluorophenyl)methyl]-1H-pyrrole
Reaktionsgleichung
[F:1][C:2]1[CH:9]=[C:8]([F:10])[CH:7]=[CH:6][C:3]=1[CH2:4][NH2:5].CO[CH:13]1[CH2:17][CH2:16][CH:15](OC)O1>>[F:1][C:2]1[CH:9]=[C:8]([F:10])[CH:7]=[CH:6][C:3]=1[CH2:4][N:5]1[CH:13]=[CH:17][CH:16]=[CH:15]1Komponenten
3
Versuchsvorschrift
8.6 g (0.060 mol) of 2,4-difluorobenzylamine are heated in an autoclave with 8 g (0.060 mol) of 2,5-dimethoxytetrahydrofuran for 2 hours at 250° C. The reaction mixture is cooled and then purified by vacuum distillation. 9.2 g (79% of theory) of a colourless oil which boils at 110°-114° C. at 16 mbar are obtained.
Aufarbeitung
- temperatureThe reaction mixture is cooled
- distillationpurified by vacuum distillation
- custom9.2 g (79% of theory) of a colourless oil which boils at 110°-114° C. at 16 mbar are obtained
Quellen und Nachweise
- ORD-Eintrag
- ord-b6de5b098cbb4f6f89e8fc2cda5786bc
- Quelldatensatz
- uspto-grants-1991_11
- Patentnummer
- US05068371
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