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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 518953생성일: 2026년 10월 27일

Nitric Acid → 4-Bromo-2-nitro-5-(trifluoromethyl)phenol

https://huagongshe.com/reaction/518953

반응식

참여 물질

역할이름HCID투입량
반응물Nitric AcidHCID 944—
반응물Sulfuric AcidHCID 1118—
반응물4-Bromo-3-(trifluoromethyl)phenolHCID 22277307—
용매Acetic AcidHCID 176—
생성물4-Bromo-2-nitro-5-(trifluoromethyl)phenolHCID 8672729936.7%

반응 단계

To a 0° C. mixture of 4-bromo-3-(trifluoromethyl)phenol (Apollo, 10.8 g, 44.8 mmol) in AcOH (40 mL) was added concentrated sulfuric acid (1.5 mL) followed by fuming nitric acid (5.2 g) and the mixture was stirred for 30 min. Additional concentrated sulfuric acid (9 mL) was added and the temperature was allowed to rise to ambient temperature and stirred for 3 h at rt. The mixture was poured into ice water (500 mL) and the aqueous solution was extracted with EtOAc (3×50 mL). The combined organic phase was washed with brine (50 mL), dried over anhydrous Na2SO4 and filtered. The filtrate was evaporated in vacuo and the residue was purified by column chromatography on silica gel (eluting with 10-20% EtOAc in petroleum ether) to give 4-bromo-2-nitro-5-(trifluoromethyl)phenol (4.7 g, 36%) as yellow oil. 1H NMR (DMSO-d6, 400 MHz): δ 12.0 (brs, 1H), 8.31 (s, 1H), 7.54 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09115151B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-e0aafc41fd6b4e37bc414a44f40c6d0e
출처 메모uspto-grants-2015_08