Chloroacetyl chloride → 2-Chloro-1-(1-methyl-1H-pyrrol-2-yl)-ethanone
Reaktionsgleichung
[CH3:1][N:2]1[CH:6]=[CH:5][CH:4]=[CH:3]1.[Cl:7][CH2:8][C:9](Cl)=[O:10]>C1COCC1>[Cl:7][CH2:8][C:9]([C:3]1[N:2]([CH3:1])[CH:6]=[CH:5][CH:4]=1)=[O:10]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of 15 g (0.186 mole) N-methylpyrrole and 19.2 mL (0.186 mole) chloroacetyl chloride in 600 mL dry THF was heated under reflux overnight with a nitrogen stream bubbling through the reaction mixture. After cooling, the organics were washed with water, 1N NaOH, water, brine and dried (MgSO4). Evaporation of the solvent gave 31.2 g of a green solid: mp (decomp.) 280° C.; NMR 300 MHz (CDCl3) d 7.05 (d, 1H); 6.95 (s, 1H); 6.2 (m, 1H); 4.5 (s, 2H); 3.9 (s, 3H).
Aufarbeitung
- temperatureunder reflux overnight with a nitrogen stream
- custombubbling through the reaction mixture
- temperatureAfter cooling
- washthe organics were washed with water, 1N NaOH, water, brine
- dry with materialdried (MgSO4)
- customEvaporation of the solvent
Quellen und Nachweise
- ORD-Eintrag
- ord-c5b2aef87b6b4b58b512059d3ec68287
- Quelldatensatz
- uspto-grants-1994_07
- Patentnummer
- US05332736
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