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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 482715생성일: 2026년 10월 26일

4-Hydroxybenzaldehyde → 4-(2,2,2-Trifluoroethoxy)benzaldehyde

https://huagongshe.com/reaction/482715

반응식

참여 물질

역할이름HCID투입량
반응물4-HydroxybenzaldehydeHCID 126—
반응물Potassium HydroxideHCID 14797—
반응물18-Crown-6HCID 28557—
반응물Ethanol, 2,2,2-trifluoro-, 1-(4-methylbenzenesulfonate)HCID 67942—
용매DiglymeHCID 8150—
생성물4-(2,2,2-Trifluoroethoxy)benzaldehydeHCID 477094630.1%

반응 단계

Potassium hydroxide pellets (85%, 13.2 g, 0.2 mol) are added to 4-hydroxybenzaldehyde (24.4 g, 0.2 mol) and 18-crown-6 (2.6 g, 5% mol) in diglyme (150 mL). The red reaction mixture is stirred for 16 hours at room temperature and then a solution of 2,2,2-trifluoroethyl-p-toluenesulfonate (50.8 g, 0.2 mol) in diglyme (100 mL) is added over 30 minutes, after which the mixture is allowed to stir at room temperature for 45 minutes. The resulting suspension is then heated at reflux for 24 hours. The mixture is cooled to 10° C. and poured into ice water (1300 mL). The organic materials are extracted with ether (4×200 mL), and the extracts washed with 5% sodium hydroxide (2×100 mL), water (2×100 mL) and saturated sodium chloride (1×100 mL), and dried over MgSO4. Evaporation of the ether gives an amber oil which is purified by high performance liquid chromatography using silica gel on a Waters 500 unit and 50:50 hexane and methylene chloride as eluant to give 12.3 g of the title product with Rf 0.25. Anal. Calcd for C9H7F3O2 (204.15) C, 52.94; H, 3.43. Found C, 52.04; H, 3.59.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04575560
출처 데이터셋uspto-grants-1986_03
ORD IDord-6770dc6d28744c09bf7f645291d24b0a
출처 메모uspto-grants-1986_03