Dimethylamine → beta-Alanine, N,N-dimethyl-, ethyl ester
Reaktionsgleichung
[CH3:1][NH:2][CH3:3].[C:4]([O:8][CH2:9][CH3:10])(=[O:7])[CH:5]=[CH2:6].C1C2NC3C(=CC=CC=3)SC=2C=CC=1.COC1C=CC(O)=CC=1>>[CH3:1][N:2]([CH2:6][CH2:5][C:4]([O:8][CH2:9][CH3:10])=[O:7])[CH3:3]Komponenten
5
Reaktionsbedingungen
- Temperatur
- -13 °C
Versuchsvorschrift
To a chilled (-15° C.) reaction vessel there was added; anhydrous dimethylamine (100 grams); ethyl acrylate (250 grams); phenothiazine (0.5 gram); and p-methoxyphenol (0.5 gram). The mixture was maintained at -13° C. for two hours with stirring after which the temperature was allowed to rise to about 25° C. Unreacted dimethylamine and ethyl acrylate were removed by distillation. The product was recovered by distillation at 58° C. and 10 mm. mercury pressure in a yield of 97 percent. The product, designated herein as Amine Catalyst VIII, has the formula, (CH3)2NCH2CH2C(O)OC2H5, as verified analytically by infrared spectroscopy.
Aufarbeitung
- temperatureTo a chilled
- custom(-15° C.) reaction vessel there
- additionwas added
- customto rise to about 25° C
- customwere removed by distillation
- distillationThe product was recovered by distillation at 58° C.
Quellen und Nachweise
- ORD-Eintrag
- ord-583a00724ed648d7843cecf34a3a456d
- Quelldatensatz
- uspto-grants-1977_03
- Patentnummer
- US04011223
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