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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1254998Erstellt: 27. Oktober 2026

Ethanol → 3-[1-(2,3-Dichlorophenoxy)-3-methylsulfanylpropyl]pyrrolidine

https://huagongshe.com/reaction/1254998

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktSodium hydrideHCID 24758—
EduktBenzene, 1,2-dichloro-3-fluoro-HCID 119011—
Edukt3-(1-Hydroxy-3-methylsulfanylpropyl)pyrrolidine-1-carboxylic Acid t-Butyl EsterHCID 66859760—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-[1-(2,3-Dichlorophenoxy)-3-methylsulfanylpropyl]pyrrolidineHCID 58120263—

Reaktionsschritte

3-(1-Hydroxy-3-methylsulfanylpropyl)pyrrolidine-1-carboxylic acid t-butyl ester (49 mg, 180 mmol) was dissolved in DMF (550 μL). 60% NaH in oil (60:40, NaH:mineral oil, 8.5 mg, 210 μmol) was slowly added, and the mixture was stirred for 15 minutes at room temperature. 1,2-Dichloro-3-fluorobenzene (62 μL, 530 μmol) was added, and the resulting mixture was heated at 90° C. for 24 hours. The reaction was quenched with MeOH, and DMF/MeOH was removed in vacuo. The product was dissolved in 1.25M HCl in EtOH (1.4 mL, 1.8 mmol) and stirred overnight at room temperature. The product was then purified by preparative HPLC to yield the title compound as a mixture of all 4 stereoisomers (R,R, R,S, S,S, and S,R) as mono-TFA salts (20 mg, 100% purity). MS m/z: [M+H]+ calcd for C14H19Cl2NOS, 320.06. found 320.0.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08455665B2
Quelldatensatzuspto-grants-2013_06
ORD IDord-f292b0e4231d40778223fddf3fe3aa8c
Quellennotizuspto-grants-2013_06