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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1740966Generated: October 25, 2026

Ethyl Acetate → 3-(5-ethyl-2-pyridinyl)-2,2-dimethyl-2,3-dihydro-(4H)-1,3-benzoxazin-4-one

https://huagongshe.com/reaction/1740966

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPyridine, 3-ethyl-, 1-oxideHCID 84685—
Reactant4-chloro-2,2-dimethyl-2H-1,3-benzoxazineHCID 602084—
SolventDichloromethaneHCID 6344—
Product3-(5-ethyl-2-pyridinyl)-2,2-dimethyl-2,3-dihydro-(4H)-1,3-benzoxazin-4-oneHCID 2183440933%

Reaction Steps

A solution of 172 mg (0.87 mmol) of 4-chloro-2,2-dimethyl-(2H)-1,3-benzoxazine (K. Wachi and A. Terada, Chem. Pharm. Bull, 1980, 28, 465-472) and 215 mg (1.75 mmol) of 3-ethylpyridine N-oxide (S. Hibino and E. Sugino, J. Heterocycl Chem., 1990, 27, 175) in 1.6 mL of methylene chloride was heated to reflux for 9 h with stirring. After cooling the reaction, 30 mL ethyl acetate was added and the mixture was washed in succession with 10 mL saturated sodium bicarbonate and 10 mL of saturated aqueous sodium chloride. The organic solution was dried (sodium sulfate), decanted, and evaporated to give a yellow liquid. Flash column chromatography on 17 g of silica gel, eluting with 100 mL of 5% ethyl acetate/hexane and 500 mL of 7% ethyl acetate/hexane furnished 84 mg (33% yield) of 3-(5-ethyl-2-pyridinyl)-2,2-dimethyl-2,3-dihydro-(4H)-1,3-benzoxazin-4-one as a colorless syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05972975
Source datasetuspto-grants-1999_10
ORD IDord-371d704204f246d19d9a55bfd8ea0d24
Source noteuspto-grants-1999_10