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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1176065Generated: November 1, 2026

M-Cresol → (3'S)-1'-[4-(3-methylphenoxy)benzoyl]-1,3'-bipyrrolidine hydrochloride

https://huagongshe.com/reaction/1176065

Reaction equation

Participants

RoleNameHCIDCharge
ReactantM-CresolHCID 342—
ReactantDichloromethaneHCID 6344—
ReactantPotassium CarbonateHCID 11430—
Reactant(S)-1,3'-Bipyrrolidin-1'-YL(4-fluorophenyl)methanoneHCID 59725829—
SolventDimethylformamideHCID 6228—
Product(3'S)-1'-[4-(3-methylphenoxy)benzoyl]-1,3'-bipyrrolidine hydrochlorideHCID 67141368—

Reaction Conditions

Temperature150 °C

Reaction Steps

A solution of (3′S)-1′-(4-fluorobenzoyl)-1,3′-bipyrrolidine (0.011 g, 0.381 mmol in dimethylformamide was treated with m-cresol (0.127 g, 1.14 mmol) and potassium carbonate (0.105 g, 0.762 mmol), heated to 150° C. via microwave radiation for 20 minutes and cooled to room temperature. The reaction mixture was diluted with dichloromethane, washed sequentially with water and saturated aqueous sodium chloride, dried over magnesium sulfate and concentrated in vacuo. The resultant residue was purified by flash column chromatography (silica, methanol:dichloromethane 5:95) to give the free amine of the title product as a yellow oil. This oil was dissolved in isopropanol and diethyl ether (1:10), treated with 1.0N HCl in diethyl ether and filtered. The filter cake was dried to afford the title product as a yellow solid, 0.021 g (16%), identified by NMR and mass spectral analyses. MS [351.3 m/e (M+H)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842715B2
Source datasetuspto-grants-2010_11
ORD IDord-3c01488734b846c89c0b823403ce476f
Source noteuspto-grants-2010_11