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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 894413Erstellt: 24. Oktober 2026

2-Butene, 1-bromo-3-methyl- → 2-Methoxy-3-(3-methyl-2-butenyl)-2,4,4-trimethyloxazolidine

https://huagongshe.com/de/reaction/894413

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Butene, 1-bromo-3-methyl-HCID 70092—
Edukt4,5-Dihydro-2,4,4-trimethyloxazoleHCID 74496—
EduktSodium MethoxideHCID 10942334—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-Methoxy-3-(3-methyl-2-butenyl)-2,4,4-trimethyloxazolidineHCID 2047426086%

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

226 g (2 mols) of 2,4,4-trimethyloxazoline were dropped at room temperature to 298 g (2 mols) 3-methyl-2-butenyl bromide in 400 ml absolute methylenchloride and were stirred for 12 hours at 20° C. After cooling to 0° C. 400 ml (2 mols) of a 30% solution of sodium methylate were added and the mixture was stirred for a further hour at room temperature. The solution was filtered and after removing off the solvent the residue was distilled. 368 g (1.72 mols, 86%) of 2-methoxy-3-(3-methyl-2-butenyl)-2,4,4-trimethyloxazolidine of boiling point 70°-76° C./0.05 mm Hg were obtained. NMR (CDCL3): α1.1 (s, 3H); 1.2 (s, 3H); 1.4 (s, 3H); 1.6-1.7 (bs, 6H); 3.2 (s, 3H); 3.25 (d, J=6.5 Hz, 2H); 3.65 (s, 2H); 5.25 (t, J=6.5 Hz, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04283544
Quelldatensatzuspto-grants-1981_08
ORD IDord-6cd0ad6f5b514f64a5ccdac555488191
Quellennotizuspto-grants-1981_08