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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711550Generated: October 31, 2026

Pyridine → HCID 23071203, compound

https://huagongshe.com/reaction/1711550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthyl AcetateHCID 8857—
ReactantEthyl chloroformateHCID 10928—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
ProductHCID 23071203HCID 23071203—

Reaction Steps

To a mixture of tert-butyl 2-hydroxyethyl (methyl)carbamate (1.75 g) obtained in Reference Example 1 and ethyl acetate (20 mL) were added pyridine (0.97 mL) and 4-dimethylaminopyridine (catalytic amount), and ethyl chlorocarbonate (1.25 mL) was dropwise added. The mixture was stirred overnight at room temperature and ethyl acetate (50 mL) was added. The mixture was washed with water (50 mL), a 5% aqueous citric acid solution (50 mL) and saturated brine (50 mL), and dried over anhydrous magnesium sulfate. After concentration under reduced pressure, a 4N hydrogen chloride—ethyl acetate solution (10 mL) was added to the residue. After stirring at room temperature for 2 hrs., diethyl ether (10 mL) was added, and the precipitated solid was collected by filtration. The solid was dried under reduced pressure to give the title compound (1.66 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790755B2
Source datasetuspto-grants-2010_09
ORD IDord-a0c11244ec2349979198371094be64e5
Source noteuspto-grants-2010_09