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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1165672Erstellt: 25. Oktober 2026

Ethanol → 1,3-Dimethoxy-2-methylpropan-2-amine

https://huagongshe.com/reaction/1165672

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktMethyl iodideHCID 6328—
EduktSodium hydrideHCID 24758—
Edukt2-Amino-3-methoxy-2-methylpropan-1-olHCID 13375415—
LösungsmittelDiethyl EtherHCID 3283—
Produkt1,3-Dimethoxy-2-methylpropan-2-amineHCID 2006587068,3%

Reaktionsschritte

To a 3-necked 3 L RB flask equipped with overhead stirrer, condenser and N2 inlet line was added NaH (Morton Thiokol, Inc. - Alfa Products, 60% in mineral oil, 44 g, 1.1 mol). After washing with hexane (3×200 mL), dry THF (1.1 L) was added to the flask. After cooling to 0°, 2-amino-3-methoxy-2-methyl-1-propanol (61C, 119.16 g, 1.0 mol) was added dropwise to the flask at such a rate that the reaction temperature remained below 30°. The resulting slurry was cooled to 0°. Iodomethane (Aldrich, 141.94 g, 1.0 mol, 62.25 mL) was added dropwise to the mixture at such a rate that the reaction temperature remained below 30°. After the mixture was stirred for 1 h, EtOH (25 mL) was added to quench the reaction. The volume of the reaction was reduced to 200 mL. This material was diluted to 2 L with Et2O, filtered and the solvent removed. Fractional distillation of this material gave 91.02 g (68.3% yield of 1,1-bis-(methoxymethyl)ethylamine, bp 146°-149°, (C,H,N).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04910218
Quelldatensatzuspto-grants-1990_03
ORD IDord-e04fa9e53e2f4a9f98a009dd38d368b1
Quellennotizuspto-grants-1990_03