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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694394Generated: November 1, 2026

Potassium Carbonate → HCID 67278856, compound

https://huagongshe.com/reaction/1694394

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(2R)-2-methylpyrrolidine hydrobromideHCID 12444175—
Reactant4-Bromo-1-(bromomethyl)-2-chlorobenzeneHCID 21914486—
SolventDimethylformamideHCID 6228—
ProductHCID 67278856HCID 6727885679%

Reaction Steps

Intermediate 3, 4-bromo-1-(bromomethyl)-2-chlorobenzene (15.4 g, 55 mmol) was added to a mixture of (2R)-2-methylpyrrolidine HBr (9.0 g, 55 mmol), potassium carbonate (18 g, 130 mmol), and 150 mL of dimethylformamide under ice cooling. The mixture was allowed to reach room temperature, and the stirring was continued overnight. The mixture was evaporated. Water (400 mL) was added followed by addition of 5M NaHSO4 to attain pH˜2. The organic layer was separated. The aqueous phase was extracted with Et2O (2×200 mL). The organic layers were discarded. The aqueous fraction was alkalized with K2CO3 to pH˜12 and subjected to extraction with Et2O (2×300 mL). The organic layer was washed with brine, dried over anhydrous Na2SO4 (100 g), and evaporated in vacuo. The residue was distilled at 1 mmHg, bp 95° C. to give the title compound (12.25 g, 79%). LC/MS data: 289.9 and 287.9 (M)+ (calculated for C12H15BrClN 288.6). 1H NMR data (DMSO-d6): δ 7.66 (d, 1H, J=1.9 Hz, Ar—H); 7.52 (dd, 1H, J1=1.9 Hz, J2=8.0 Hz, Ar—H), 7.43 (d, 1H, J=8.1 Hz, Ar—H), 3.91 (d, 1H, J=14.4 Hz), 2.28 (d, 2H, J=8.5 Hz); 2.78-2.85 (m, 1H); 2.42-2.49 (m, 1H); 2.11 (dd, 1H, J1=8.8 Hz, J2=17.6 Hz); 1.87-1.97 (m, 1H); 1.57-1.67 (m, 2H); 1.27-1.39 (m, 1H); 1.08 (d, 3H, J=5.9 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158673B2
Source datasetuspto-grants-2012_04
ORD IDord-28e4d6399140489b8dacf566a6a2b57e
Source noteuspto-grants-2012_04