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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10338생성일: 2026년 10월 23일

Hydrochloric Acid → (7,8-Difluoro-3-methyl-2,3-dihydro-1,4-benzoxazin-4-yl)-oxoacetaldehyde oxime

https://huagongshe.com/ko/reaction/10338

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Chloral HydrateHCID 2707—
반응물Sodium sulfate decahydrateHCID 62649—
반응물Hydroxyamine hydrochlorideHCID 443297—
반응물7,8-Difluoro-2,3-dihydro-3-methyl-4H-(1,4)benzoxazineHCID 10219718—
용매WaterHCID 962—
생성물(7,8-Difluoro-3-methyl-2,3-dihydro-1,4-benzoxazin-4-yl)-oxoacetaldehyde oximeHCID 73857481—

반응 조건

온도77.5 °C

반응 단계

A solution of 8.27 g (50 mmol) of chloral hydrate in 125 mL of water is treated with 112.8 g (0.35 mmol) of sodium sulfate decahydrate. The mixture is stirred and treated with a solution of 7,8-difluoro-3-methyl-3,4-dihydro-2H-benz[1,4]oxazine (Chem. Pharm. Bull., 1984; 32:4907) hydrochloride (prepared by dissolving 8.26 g (44.6 mmol) of the free base in 50 mmol of concentrated hydrochloric acid in 70 mL of 50% aqueous ethanol). The reaction is stirred and a solution of 9.8 g (140 mmol) of hydroxylamine hydrochloride in 50 mL of water is added. After heating at 75 to 80° C. for 3 hours, the reaction is stirred at room temperature overnight. The resulting precipitate is removed by filtration, washed with water, and the wet filter cake is dissolved in dichloromethane. The organic solution is washed with water, dried (MgSO4), decolorized with charcoal, filtered and concentrated in vacuo to give 10.5 g of the title compound, mp 188–190° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094780B1
출처 데이터셋uspto-grants-2006_08
ORD IDord-b845dd2edd604c6ea501e182a83263a2
출처 메모uspto-grants-2006_08