Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 60403Erstellt: 24. Oktober 2026

Dimethyl Sulfate → 2,2-Dimethoxy-1-methylpyrrolidine

https://huagongshe.com/de/reaction/60403

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfateHCID 6497—
EduktN-methyl-2-pyrrolidoneHCID 13387—
EduktSodium MethoxideHCID 10942334—
LösungsmittelMethanolHCID 887—
Produkt2,2-Dimethoxy-1-methylpyrrolidineHCID 11073552—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

To a mixture containing 10 mL (10.28 g, 104 mmol) of N-methyl-2-pyrrolidinone and 10 mL (13.25 g, 105 mmol) of dimethyl sulfate was stirred and heated at 90° C. for 1.5 h, then allowed to cool to room temperature. A solution containing 25 mL of 25% methanolic sodium methoxide and 72 mL of methanol was added at −10° C. under Ar over a period of 1 h. The precipitated solid was filtered and the solvent was concentrated under diminished pressure. The residue was dissolved in 100 mL of ether and stirred for 1 h, then the precipitated solid was filtered. The solid was washed with two 10-mL portions of ether. After concentration under diminished pressure, the residue was distilled in vacuo to give 2,2-dimethoxy-1-methylpyrrolidine as a yellow liquid: yield 4.42 g (29%); 1H NMR (CDCl3) δ 1.62-1.74 (m, 2H), 1.83 (t, 2H, J=7.8 Hz), 2.28 (s, 3H), 2.78 (t, 2H, J=6.6 Hz), 3.15 (s, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09440967B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-0ab3344e38254bd8b1a434f63f4d62d8
Quellennotizuspto-grants-2016_09