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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370610Generated: November 1, 2026

Pyridine → HCID 57104612, compound

https://huagongshe.com/reaction/1370610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantChloromethyl chloroformateHCID 62754—
Reactant(R)-SolketalHCID 736056—
SolventDiethyl EtherHCID 3283—
ProductHCID 57104612HCID 57104612100%

Reaction Steps

(R)-Glycerol acetonide (10 g) was dissolved in anhydrous ether (200 ml) and, after adding pyridine (6.6 g) at −10° C., a solution of chloromethyl chloroformate (10.7 g) in anhydrous ether (20 ml) was added dropwise over the period of 10 minutes. After the reaction mixture 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 (200 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: hexane→ethyl acetate/hexane=1/5 →ethyl acetate/hexane=3/5) to obtain chloromethyl [(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]methyl carbonate (17 g) as a colorless oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06583164B1
Source datasetuspto-grants-2003_06
ORD IDord-d3909f49b94a486ba7a10128dc04f64a
Source noteuspto-grants-2003_06