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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 21753Erstellt: 24. Oktober 2026

Formaldehyde → (S)-Methyl 1-methylpyrrolidine-2-carboxylate

https://huagongshe.com/de/reaction/21753

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormaldehydeHCID 712—
EduktSulfuric AcidHCID 1118—
EduktPotassium CarbonateHCID 11430—
EduktL-ProlineHCID 145742—
EduktSodium borohydrideHCID 4311764—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
Produkt(S)-Methyl 1-methylpyrrolidine-2-carboxylateHCID 10920622—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Methanol (2.2 L, 68.66 mol) was stirred under nitrogen and cooled to 0° C. Sulfuric acid (97%, 0.179 L, 3.26 mol) was added with vigorous stirring at a rate such that the internal temperature of the reactor did not rise above 10° C. L-Proline (0.5 kg, 4.34 mol) was added to the methanol, and the reaction was refluxed for 18 hr. The reaction mixture was cooled to 0° C., and with vigorous stirring a solution of K2CO3 (0.217 kg, 1.57 mol) in 0.363 L of water was slowly added to the mixture, until the pH was between pH 7 and 8. The neutralized solution was again cooled to 0° C., and aqueous formaldehyde solution (36%, 0.543 L) was added. After stirring for 15 min, 0.082 kg (2.17 mol) of powdered sodium borohydride was added in portions while maintaining the temperature between -5° and +5° C. The suspension was stirred for 3 hr, then filtered, and the filter cake was washed with toluene. The combined organic solvents were diluted 1:1 with water (2.6 L) and filtered. The organic phase was separated, and the aqueous layer was extracted at 0° C. with 5×0.5 L portions of toluene. The toluene extracts were combined, dried over sodium sulfate and filtered. The volume of the solution was reduced by half by distillation at 60° C. and 90 mbar pressure. The solution was taken to the next step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05424444
Quelldatensatzuspto-grants-1995_06
ORD IDord-545a2659e6fa4d5da251bc882e1a77a2
Quellennotizuspto-grants-1995_06