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HRID 1740966생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1740966

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Pyridine, 3-ethyl-, 1-oxideHCID 84685—
반응물4-chloro-2,2-dimethyl-2H-1,3-benzoxazineHCID 602084—
용매DichloromethaneHCID 6344—
생성물3-(5-ethyl-2-pyridinyl)-2,2-dimethyl-2,3-dihydro-(4H)-1,3-benzoxazin-4-oneHCID 2183440933%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05972975
출처 데이터셋uspto-grants-1999_10
ORD IDord-371d704204f246d19d9a55bfd8ea0d24
출처 메모uspto-grants-1999_10