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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448193Generated: October 30, 2026

Pyridine → HCID 68738533, compound

https://huagongshe.com/reaction/448193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant3-HydroxyacetophenoneHCID 8487—
Reactant2,6-Dimethylbenzoyl chlorideHCID 89096—
SolventDichloromethaneHCID 6344—
ProductHCID 68738533HCID 68738533—

Reaction Steps

To a stirred solution of 3′-Hydroxyacetophenone (4.84 g, 35.5 mmol) in anhydrous CH2Cl2 (50 ml) was added at room temperature pyridine (25 ml) followed by addition of 2,6-Dimethylbenzoyl chloride (Step A, 6 g, 35 mmol) in anhydrous CH2Cl2 (10 ml) under argon. The reaction mixture was stirred for 16 hours, concentrated under reduced pressure, diluted with CH2Cl2, and washed with 0.1M HCl, water and brine. The organic layer was dried over Na2SO4, concentrated and purified by flash chromatography eluted with ethyl acetate:hexane (1:2) to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481595B2
Source datasetuspto-grants-2013_07
ORD IDord-81103bde3acf4accb36a3c2f4a275294
Source noteuspto-grants-2013_07