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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1257478생성일: 2026년 10월 27일

Ammonium Chloride → Ethyl 4-(hydroxy{5-[3-(trifluoromethyl)phenyl]furan-2-yl}methyl)benzoate

https://huagongshe.com/reaction/1257478

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물Ethyl 4-iodobenzoateHCID 142891—
반응물5-(3-(Trifluoromethyl)phenyl)furfuralHCID 721837—
반응물HCID 178418918HCID 178418918—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 4-(hydroxy{5-[3-(trifluoromethyl)phenyl]furan-2-yl}methyl)benzoateHCID 6693973740%

반응 조건

온도-40 °C

반응 단계

Ethyl 4-iodobenzoate (0.55 g) was dissolved in tetrahydrofuran (5 mL), and the mixture was cooled to −40° C. Isopropylmagnesium chloride (2M tetrahydrofuran solution, 1.0 mL) was added dropwise, and the mixture was stirred at the same temperature for 30 min to prepare Grignard reagent. A solution of the compound (0.40 g) obtained in Example 222a in tetrahydrofuran (5 mL) was cooled to −40° C., and the prepared Grignard reagent solution was added. After stirring at −40° C. for 30 min, saturated aqueous ammonium chloride solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by column chromatography (carrier: silica gel, eluent: hexane-ethyl acetate) to give the title compound (0.26 g) as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08461348B2
출처 데이터셋uspto-grants-2013_06
ORD IDord-22735f51bfc0455292c94bdbd945b1b3
출처 메모uspto-grants-2013_06