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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25144생성일: 2026년 10월 25일

Chloroacetyl chloride → 6-Nitro-2H-1,4-benzoxazin-3(4H)-one

https://huagongshe.com/reaction/25144

반응식

참여 물질

역할이름HCID투입량
반응물Chloroacetyl chlorideHCID 6577—
반응물Sodium BicarbonateHCID 516892—
반응물2-Amino-4-NitrophenolHCID 3613389—
촉매Benzyl triethylammonium chlorideHCID 66133—
용매ChloroformHCID 6212—
생성물6-Nitro-2H-1,4-benzoxazin-3(4H)-oneHCID 2763683—

반응 단계

A suspension of 2-amino4-nitrophenol (7.7 g, 50 mmol) was prepared in 125 mL chloroform. To this suspension was added benzyltriethylammonium chloride (11.4 g, 50 mmol) and sodium bicarbonate (16.80 g, 200 mmol) and the suspension cooled in an ice bath. A solution of chloroacetyl chloride (4.8 mL, 60 mmol) in chloroform (10 mL) was added. The solution was stirred overnight at room temperature, then refluxed for 3 hours and again let sit overnight at room temperature. The solvent was removed under vacuum and water was added to the residue. The solid was filtered, washed with water, and recrystallized from ethanol. The recrystallized solid was filtered and washed with cold ethanol and then dried, to yield 6-nitro-4-H-benzo[1,4]oxazin-3-one as a solid product. Some additional product precipitated from the ethanol filtrate as a second crop and was recovered by filtration.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858621B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-9b19e161efe9479f8d016afeedebaf5d
출처 메모uspto-grants-2005_02