Dimethylamine → 3-(2-Hydroxyphenyl)-1,1-dimethylurea
Reaktionsgleichung
[CH:1]1[CH:2]=[CH:3][C:4]2[O:10][C:8](=[O:9])[NH:7][C:5]=2[CH:6]=1.[CH3:11][NH:12][CH3:13]>>[OH:10][C:4]1[CH:3]=[CH:2][CH:1]=[CH:6][C:5]=1[NH:7][C:8]([N:12]([CH3:13])[CH3:11])=[O:9]Komponenten
3
Versuchsvorschrift
Benzoxazolinone (200 g) was stirred with 1 liter of a 33% solution of dimethylamine in industrial alcohol at 50° C. for 48 hours. The alcohol and unchanged dimethylamine were distilled off under reduced pressure at below 60° C. and the product was recrystallised from a 1:1 by volume mixture of isopropanol and light petroleum ether (b.pt. 60°-80° C.). It melted at 148° C. (decomp.) as measured on a Kofler bench.
Aufarbeitung
- distillationThe alcohol and unchanged dimethylamine were distilled off under reduced pressure at below 60° C.
- customthe product was recrystallised from a 1:1 by volume mixture of isopropanol and light petroleum ether (b.pt. 60°-80° C.)
Quellen und Nachweise
- ORD-Eintrag
- ord-e484a090c2104e94b41ef7bed8745c54
- Quelldatensatz
- uspto-grants-1983_09
- Patentnummer
- US04404356
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