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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 722143Generated: October 31, 2026

Thionyl Chloride → 2,3-Bis(chloromethyl)pyridine

https://huagongshe.com/reaction/722143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant(Pyridine-2,3-diyl)dimethanol--hydrogen chloride (1/1)HCID 17750570—
Product2,3-Bis(chloromethyl)pyridineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138400B2
Source datasetuspto-grants-2006_11
ORD IDord-e7f22a92cc81405d9282ee06d0b5a03c
Source noteuspto-grants-2006_11