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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34983Generated: October 25, 2026

Pyridine → 2,6-Bis(chloromethyloxy-carbonyloxymethyl)pyridine

https://huagongshe.com/reaction/34983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantChloromethyl chloroformateHCID 62754—
Reactant2,6-PyridinedimethanolHCID 70957—
SolventChloroformHCID 6212—
Product2,6-Bis(chloromethyloxy-carbonyloxymethyl)pyridineHCID 1474955595%

Reaction Steps

The reaction of the compound of the formula (II) with the compound of the formula (III) is carried out at a temperature between -30° C. and +10° C., preferably at about -5° C. This reaction will be described in detail hereinafter. At least 2 moles of chloromethyl chloroformate of the formula (III) [as calculated for 2,6-bis(hydroxymethyl)pyridine of the formula (II)] are dissolved in the desired solvent, preferably in chloroform, and a solution containing an organic base, preferably pyridine, in the same molar amount as the compound of the formula (III) in the same solvent is added at a temperature lower than 10° C., preferably at about -5° C., under stirring. The suspension obtained is stirred for about 20 minutes while care is taken to avoid any increase of the temperature. Then, 2,6-bis(hydroxymethyl)pyridine of the formula (II) is added to the above mixture at the same temperature at such a rate that the temperature reaches at most -5° C. The suspension is stirred for about 20 minutes to give a brown solution. After washing this solution with water and evaporation, a practically pure product with 95 to 97% of 2,6-bis(chloromethyloxy-carbonyloxymethyl)pyridine content is obtained. The product obtained after washing with water and making free of the solvent can be used without any purification or, if desired, may be further purified by chromatography on a silicagel column or on an other adsorbent, e.g. on a synthetic resin.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04764613
Source datasetuspto-grants-1988_08
ORD IDord-d0a7d882a5dc4a7cae8c601d5f4403b6
Source noteuspto-grants-1988_08