HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373378Generated: October 25, 2026
Phosphorus pentachloride → 4'-Chloro-2,2':6',2''-terpyridine
https://huagongshe.com/reaction/1373378
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | 2,6-Bis(2-pyridyl)-4(1H)-pyridone | HCID 619353 | — |
| Solvent | Phosphorus oxychloride | HCID 24813 | — |
| Product | 4'-Chloro-2,2':6',2''-terpyridine | HCID 667748 | — |
Reaction Steps
A mixture of 3.99 g (16 mmol) of 1′H-[2,2′;6′,2″]terpyridin-4′-one (L1) and 8.0 g (38 mmol) of phosphorus pentachloride is boiled at reflux in 200 ml of phosphorus oxychloride for sixteen hours. The mixture is allowed to cool and concentrated to dryness. 200 ml of ice-water are then added cautiously to the residue, and the solution is then adjusted to pH 9 with aqueous potassium hydroxide solution. Extracton is carried out three times using chloroform and the organic extracts are dried over sodium sulfate, filtered and concentrated. After recrystallisation from ethanol, 4′-chloro-[2,2′;6′,2″]terpyridine is obtained in the form of white needles. 1H-NMR (CDCl3, 360 MHz): 7.20–7.29 (m, 2H); 7.70–7.79 (tm, 2H); 8.37 (s, 2H); 8.47 (d, 2H; 7.6 Hz); 8.56–8.63 (dm, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07161005B2 |
|---|
| Source dataset | uspto-grants-2007_01 |
|---|
| ORD ID | ord-3653ddffd74140168f7cc0c3dd0b06fe |
|---|
| Source note | uspto-grants-2007_01 |
|---|