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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1030149Erstellt: 25. Oktober 2026

Acetic Acid → (3S)-3-(4-Methoxybenzylthio)-1-methylpyrrolidine

https://huagongshe.com/reaction/1030149

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktFormaldehydeHCID 712—
EduktEthyl AcetateHCID 8857—
Edukt(3S)-3-(4-methoxybenzylthio)pyrrolidineHCID 14880282—
LösungsmittelWaterHCID 962—
LösungsmittelAcetonitrileHCID 6342—
Produkt(3S)-3-(4-Methoxybenzylthio)-1-methylpyrrolidineHCID 57243155—

Reaktionsschritte

750 mg of (3S)-3-(4-methoxybenzylthio)pyrrolidine [which had been prepared by neutralization of 900 mg of (3S)-3-(4-methoxybenzylthio)pyrrolidine hydrochloride, prepared as described in step (3) above, with sodium bicarbonate] were dissolved in 15 ml of dry acetonitrile, and 1.44 ml of a 35% by volume solution of formaldehyde in water was added to the solution. The reaction mixture was then stirred for 15 minutes, after which it was neutralized by the addition of acetic acid; it was then again stirred for a further 2.5 hours. At the end of this time, the reaction mixture was poured into 200 ml of ethyl acetate, and the mixture was washed with a 2N aqueous solution of potassium hydroxide and an aqueous solution of sodium chloride. The organic layer was dried over potassium carbonate and the solvent was distilled off under reduced pressure. The residue was purified by column chromatography through silica gel (eluted with a 3:1 by volume mixture of ethyl acetate and methanol), to afford 349 mg of the title compound as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05104867
Quelldatensatzuspto-grants-1992_04
ORD IDord-15ea8125c7bd4efcb6fbffe313c03027
Quellennotizuspto-grants-1992_04