HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 3-(chloromethyl)-2-ethylPyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (2-Ethylpyridin-3-yl)methanol | HCID 19690951 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(chloromethyl)-2-ethylPyridine | HCID 19690958 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
The 2-ethyl-3-hydroxymethylpyridine (2.3 g, 16.8 mmol) was dissolved in CH2Cl2 (100 mL) and cooled under nitrogen to 0° C. and thionyl chloride (7.0 mL) was slowly added and the reaction was stirred for 3 hours. The solvent was removed under reduced pressure and the residue was partitioned between CH2Cl2 (100 mL) and saturated aqueous sodium bicarbonate (100 mL). The organic layer was dried with MgSO4, filtered, and the solvent removed under reduced pressure to give the desired 2-ethyl-3-chloromethylpyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05726172 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-090d23f63738479ca8c99ffd51c34f39 |
| Source note | uspto-grants-1998_03 |