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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726864Generated: October 30, 2026

Pyridine → HCID 54454033, compound

https://huagongshe.com/reaction/726864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPivaloyl chlorideHCID 62493—
ReactantHCID 22861808HCID 22861808—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 54454033HCID 54454033—

Reaction Steps

To a solution of 70 from Example 69, being 60.2 mg in 4 ml methylene chloride and 200 ml pyridine was added 15 mg DMAP (4-dimethylaminopyridine) followed by 68.66 mg pivaloyl chloride, i.e., trimethyl acetyl chloride. After stirring for 24 hours, the reaction mixture was diluted with ethyl acetate, washed with water, then aqueous sodium carbonate and brine. The organic layer was dried, concentrated to a residue, which was purified by preparative chromatography on silica gel using 3:1 chloroform/acetone as eluant to yield pure title compound 71 Proton NMR confirmed the assigned structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05710275
Source datasetuspto-grants-1998_01
ORD IDord-164a26b0573449cd862b7c1673e6b344
Source noteuspto-grants-1998_01