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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 452573생성일: 2026년 10월 25일

Hydroxyamine hydrochloride → N-hydroxy-1-(1-methyl-1H-tetrazol-5-yl)-1-[3-(trifluoromethoxy)phenyl]methanimine

https://huagongshe.com/reaction/452573

반응식

참여 물질

역할이름HCID투입량
반응물Hydroxyamine hydrochlorideHCID 443297—
반응물(1-methyl-1H-tetrazol-5-yl)[3-(trifluoromethoxy)phenyl]methanoneHCID 67075092—
용매PyridineHCID 1049—
용매Ethyl AcetateHCID 8857—
생성물N-hydroxy-1-(1-methyl-1H-tetrazol-5-yl)-1-[3-(trifluoromethoxy)phenyl]methanimineHCID 13633738592%

반응 조건

온도70 °C

반응 단계

To a stirred solution of (1-methyl-1H-tetrazol-5-yl)[3-(trifluoromethoxy)phenyl]methanone (5.12 g, 16.2 mmol) in dry pyridine (25 mL) was added hydroxylamine hydrochloride (2.81 g, 40.4 mmol). The mixture was stirred at 70° C. for 3 h, then left to stand overnight. After concentration of the reaction mixture in vacuo, the residue was diluted with ethyl acetate (100 mL) and washed with water (50 mL). The aqueous layer was extracted with ethyl acetate (50 mL), the combined organic layers dried (MgSO4), concentrated in vacuo and dissolved in toluene. A crystalline precipitate appeared, which was filtered off to afford N-hydroxy-1-(1-methyl-1H-tetrazol-5-yl)-1-[3-(trifluoromethoxy)phenyl]methanimine as a white solid [4.33 g, yield 92%; HPLC/MS:m/z=288 (M+H); log P(HCOOH)=2.37].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08492388B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-9a719dbbe32c4adcb817e72b8d34ec10
출처 메모uspto-grants-2013_07