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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2070029생성일: 2026년 10월 27일

Allyl Alcohol → 3-(4-Nitro-2-(trifluoromethyl)phenyl)propionaldehyde

https://huagongshe.com/reaction/2070029

반응식

참여 물질

역할이름HCID투입량
반응물Allyl AlcoholHCID 7858—
반응물TriethylamineHCID 8471—
반응물2-Bromo-5-nitrobenzotrifluorideHCID 136198—
촉매Tetrabutylammonium ChlorideHCID 70681—
촉매palladium(II) acetateHCID 167845—
용매DimethylformamideHCID 6228—
생성물3-(4-Nitro-2-(trifluoromethyl)phenyl)propionaldehydeHCID 2315529669%

반응 조건

온도90 °C

반응 단계

4-Bromo-3-(trifluoromethyl)nitrobenzene (2700 mg, 10 mmol) was dissolved in DMF (15 mL), and allyl alcohol (1750 mg, 30 mmol), tetrabutylammonium chloride (2780 mg, 10 mmol), palladium acetate (120 mg, 5 mol %), and triethylamine (3 mL, 21 mmol) were added thereto. The resulting mixture was stirred under argon atmosphere at 90° C. for 0.5 hours. The reaction solution was partitioned between water and ethyl acetate. The organic layer was washed with saturated brine and concentrated under reduced pressure. The residue was purified by silica-gel column chromatography (n-hexane:ethyl acetate=4:1) to give 3-(4-nitro-2-(trifluoromethyl)phenyl)propionaldehyde (1700 mg, 69%) as a light-yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08299252B2
출처 데이터셋uspto-grants-2012_10
ORD IDord-41d60ad3953644c4b04ae802bfc04e5a
출처 메모uspto-grants-2012_10