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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186894Generated: November 1, 2026

Pyridine → HCID 57104612, compound

https://huagongshe.com/reaction/2186894

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 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 numberUS06407129B1
Source datasetuspto-grants-2002_06
ORD IDord-69a02a3dec33447083ef55e03412451d
Source noteuspto-grants-2002_06