HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 2,3-Bis(chloromethyl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (Pyridine-2,3-diyl)dimethanol--hydrogen chloride (1/1) | HCID 17750570 | — |
| Product | 2,3-Bis(chloromethyl)pyridine | HCID 14518750 | — |
Reaction Steps
2,3-bis(hydroxymethyl)pyridine hydrochloride (JP 49 020181) (2.7 g, 15.4 mmol) was added portionwise to stirred thionyl chloride (20 mL) at 0° C. under nitrogen. The cooling bath was removed, and the reaction allowed to come to room temperature, then heated at reflux for one hour. The dark mixture was allowed to cool to room temperature, then the thionyl chloride was removed in vacuo. The residue was azeotroped with toluene (x2), the brown solid residue treated with ice, basified with Na2CO3 (sat), then extracted with diethyl ether (x3). The combined extracts were dried (Na2SO4), filtered and evaporated to give 2,3-bis(chloromethyl)pyridine (2.6 g) as a red/brown liquid. This material was used immediately in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07138400B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-e7f22a92cc81405d9282ee06d0b5a03c |
| Source note | uspto-grants-2006_11 |