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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37106생성일: 2026년 10월 25일

Sodium hydride → 2-(3,4-Dihydro-2,2-dimethyl-6-nitro-2H-1,4-benzoxazin-4-yl)pyridine N-oxide

https://huagongshe.com/reaction/37106

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물2-Bromopyridine 1-oxide hydrochlorideHCID 2724044—
반응물2,2-Dimethyl-6-nitro-3,4-dihydro-2H-benzo[B][1,4]oxazineHCID 10727057—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물2-(3,4-Dihydro-2,2-dimethyl-6-nitro-2H-1,4-benzoxazin-4-yl)pyridine N-oxideHCID 131974—

반응 단계

In 10 ml of N,N-dimethylformamide was dissolved 2.66 g of 3,4-dihydro-2,2-dimethyl-6-nitro-2H-1,4-benzoxazine followed by addition of 1.02 g of sodium hydride (60% in oil) and the mixture was stirred at room temperature for 30 minutes. Then, 2.77 g of 2-bromopyridine N-oxide hydrochloride was added with ice-cooling and, after the evolution of heat had subsided, the mixture was stirred at room temperature for 2 hours. The reaction mixture was then poured in water and extracted with ethyl acetate. The organic layer was separated and dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure and the residue was chromatographed on a silica gel column using chloroform as the eluent to give crude 2-(3,4-dihydro-2,2-dimethyl-6-nitro-2H-1,4-benzoxazin-4-yl)pyridine N-oxide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05420126
출처 데이터셋uspto-grants-1995_05
ORD IDord-43bd8fdba5d64894acdd9bc217ce5490
출처 메모uspto-grants-1995_05