HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694394Generated: November 1, 2026
Potassium Carbonate → HCID 67278856, compound
https://huagongshe.com/reaction/1694394
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (2R)-2-methylpyrrolidine hydrobromide | HCID 12444175 | — |
| Reactant | 4-Bromo-1-(bromomethyl)-2-chlorobenzene | HCID 21914486 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67278856 | HCID 67278856 | 79% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08158673B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-28e4d6399140489b8dacf566a6a2b57e |
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| Source note | uspto-grants-2012_04 |
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