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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 21752Erstellt: 23. Oktober 2026

Dimethyl Sulfate → Methyl (2S)-1-methyl-5-oxoprolinate

https://huagongshe.com/de/reaction/21752

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfateHCID 6497—
EduktTetrahydrofuranHCID 8028—
EduktTriethylamineHCID 8471—
EduktMethyl 5-oxo-L-prolinateHCID 78646—
LösungsmittelDiethyl EtherHCID 3283—
ProduktMethyl (2S)-1-methyl-5-oxoprolinateHCID 12361160—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

The methyl ester compound from step 5a above (18.3 kg, 127.8 mol) and dimethyl sulfate (20.09 kg, 159.3 mol) were introduced into a reactor, and the mixture was heated to 60° C. under an N2 atmosphere. Heating was continued until the concentration of starting material dropped below 15%. An additional 6.25 kg (0.5 eq) of dimethyl sulfate was added with exothermic response. The thick reaction mixture was then cooled to 25° C., and a solution of triethylamine (16.12 kg) in diethyl ether (19.2 L) was added at such a rate that the temperature did not rise above 30° C. The emulsion was washed with two 50 L portions of water. The ether layer was separated, and the residue was extracted with ethyl acetate (60 l). The combined organic layers were dried over Na2SO4 and azeotroped with toluene until no more triethylamine remained in the residue. The residue was mixed with dimethyl sulfate (1.7 kg, 13.5 mol) and THF (70 L) and refluxed under nitrogen until the reaction was complete. The solvents were evaporated under vacuum, and the residue was distilled under high vacuum to yield a colorless product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05424444
Quelldatensatzuspto-grants-1995_06
ORD IDord-fdbb4594a18c4b7c882440ebfca7694a
Quellennotizuspto-grants-1995_06