HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4-Dichloropyridine → 4-Chloro-2-(3-chlorophenyl)pyridine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4-Dichloropyridine | HCID 33515 | — |
| Reactant | (3-Chlorophenyl)boronic acid | HCID 2734323 | — |
| Product | 4-Chloro-2-(3-chlorophenyl)pyridine hydrochloride | HCID 90110659 | 71.1% |
Reaction Steps
Following general procedure F, 2,4-dichloropyridine (4.0 g, 27 mmol) was reacted with (3-chlorophenyl)boronic acid (4.6 g, 30 mmol), followed by formation of the hydrochloride salt to afford the title compound (5.0 g, 71%) as a white solid. MW=260.55. 1H NMR (CDCl3, 500 MHz) δ 8.92-8.79 (m, 1H), 8.16-8.09 (m, 1H), 8.03 (s, 1H), 7.95 (s, 1H), 7.74-7.64 (m, 1H), 7.58-7.52 (m, 2H); APCI MS m/z 224 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09221843B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-258c5a656afa42c295a05a7ebfb15a12 |
| Source note | uspto-grants-2015_12 |