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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370609Generated: November 1, 2026

Pyridine → HCID 11084789, compound

https://huagongshe.com/reaction/1370609

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant1,3-Dioxolane-4-methanolHCID 21618—
ReactantChloromethyl chloroformateHCID 62754—
SolventDiethyl EtherHCID 3283—
ProductHCID 11084789HCID 110847896.4%

Reaction Steps

Glycerol formal (14 g) was dissolved in anhydrous ether (400 ml) and, after adding pyridine (15 g) at −10° C., a solution of chloromethyl chloroformate (25 g) in anhydrous ether (50 ml) was added dropwise over the period of 10 minutes. After the reaction solution was stirred at room temperature for 20 hours, the deposited pyridine hydrochloride was removed by filtration. The filtrate was washed with a saturated sodium chloride aqueous solution (400 ml×2), and then dried over anhydrous magnesium sulfate. The residue obtained by distilling off the solvent under reduced pressure was purified by subjecting it to silica gel chromatography (eluent: ethyl acetate/hexane=1/5→ethyl acetate/hexane=1/3) to obtain chloromethyl (1,3-dioxan-5-yl) carbonate (1.7 g) as a colorless oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06583164B1
Source datasetuspto-grants-2003_06
ORD IDord-246fd93592f643e78826284aa7a2ec6a
Source noteuspto-grants-2003_06