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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1912878생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1912878

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참여 물질

역할이름HCID투입량
반응물Allyl AlcoholHCID 7858—
반응물TriethylamineHCID 8471—
반응물2-Bromo-5-nitrobenzotrifluorideHCID 136198—
촉매Tetrabutylammonium BromideHCID 74236—
촉매palladium(II) acetateHCID 167845—
용매DimethylformamideHCID 6228—
생성물3-(4-Nitro-2-(trifluoromethyl)phenyl)propionaldehydeHCID 23155296166.1%

반응 조건

온도90 °C

반응 단계

In 3 mL of dimethylformamide, 50 mg (0.19 mmol) of 4-bromo-3-(trifluoromethyl)nitrobenzene was dissolved, and 33 mg (0.56 mmol) of allyl alcohol, 43 mg (0.19 mmol) of tetrabutylammonium bromide, 2.1 mg (5 mol %) of palladium acetate and 52 μL (0.37 mmol) of triethylamine were added thereto and the mixture solution was stirred in an argon atmosphere at 90° C. for two hours. The reaction solution was partitioned between water and ethyl acetate, and the organic layer was washed with a saturated sodium chloride solution and concentrated under reduced pressure. The product was purified by a silica gel column (n-hexane:ethyl acetate=5:1) to obtain 78 mg (79%) of a target product as a pale yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08609656B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-3c38739d11ca4ac19714f837354af43e
출처 메모uspto-grants-2013_12