돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 637876생성일: 2026년 10월 25일

Hydrochloric Acid → 5-Nitro-2-hydroxybenzophenone oxime

https://huagongshe.com/reaction/637876

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Hydroxyamine hydrochlorideHCID 443297—
반응물Methanone, (2-hydroxy-5-nitrophenyl)phenyl-HCID 519604—
용매Potassium HydroxideHCID 14797—
생성물5-Nitro-2-hydroxybenzophenone oximeHCID 136258108—

반응 단계

Into an autoclave, were charged 30 g of 2-chloro-5-nitrobenzophenone, 300 ml of water, and 9.70 g of potassium hydroxide. The mixture was allowed to react at 150° to 160° C. with stirring for 5 hours. Upon cooling to room temperature, there was obtained a clear liquid, reddish orange in color. The liquid was further cooled below 0° C. and strongly acidified with cold concentrated hydrochloric acid. The precipitated solids were collected by filtration, washed with water, and recrystallized from ethanol to yield 15.7 g (56.1%) of 5-nitro-2-hydroxy-benzophenone having a melting point of 122°-123° C. To 150 ml of 40-% aqueous potassium hydroxide solution, was added 25.0 g of 5-nitro-2-hydroxybenzophenone followed by 50 g of hydroxylamine hydrochloride. After 5 hours, the resulting clear liquid was cooled and acidified with concentrated hydrochloric acid to form a precipitate. The precipitate was washed with water and a small volume of 50-% aqueous methanol, then dried in air, and recrystallized from benzene and petroleum ether to yield 5-nitro-2-hydroxybenzophenone oxime.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04559172
출처 데이터셋uspto-grants-1985_12
ORD IDord-0a6fdccfed1d47dd8b55cd0832f16062
출처 메모uspto-grants-1985_12