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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | M-Cresol | HCID 342 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (S)-1,3'-Bipyrrolidin-1'-YL(4-fluorophenyl)methanone | HCID 59725829 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (3'S)-1'-[4-(3-methylphenoxy)benzoyl]-1,3'-bipyrrolidine hydrochloride | HCID 67141368 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07842715B2 |
|---|
| Source dataset | uspto-grants-2010_11 |
|---|
| ORD ID | ord-3c01488734b846c89c0b823403ce476f |
|---|
| Source note | uspto-grants-2010_11 |
|---|