HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384645Generated: October 25, 2026
Thionyl Chloride → 3-(2-Chloroethoxy)pyridine hydrochloride
https://huagongshe.com/reaction/1384645
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-(Pyridin-3-yloxy)ethan-1-ol | HCID 21908997 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-(2-Chloroethoxy)pyridine hydrochloride | HCID 22624985 | 25.8% |
Reaction Steps
Thionyl chloride (0.89 ml, 12 mmol) was added slowly to a solution of 3-(2-hydroxyethoxy)pyridine (1.13 g, 8 mmol) in trichloromethane (20 ml) at 5° C. The mixture was stirred at 5° C. for 1 hour and then at ambient temperature for 2 hours. The volatiles were removed by evaporation, the residue azeotroped with toluene and dried under vacuum to give 3-(2-chloroethoxy)pyridine hydrochloride (300 mg, 19%) as a solid. 1H NMR Spectrum: (DMSOd6) 3.99(t, 2H); 4.42(t, 2H); 7.82(dd, 1H); 8.05(dd, 1H); 8.42(d, 1H); 8.62(s, 1H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06258951B1 |
|---|
| Source dataset | uspto-grants-2001_07 |
|---|
| ORD ID | ord-aab8ae36889b4383ae6c0a660de451db |
|---|
| Source note | uspto-grants-2001_07 |
|---|