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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1172697생성일: 2026년 10월 27일

Water → 2,5-Difluoro-4-{1-[4-methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-propoxy}-benzonitrile

https://huagongshe.com/reaction/1172697

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물2,4,5-TrifluorobenzonitrileHCID 593813—
반응물1-[4-Methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-propan-1-olHCID 23549129—
반응물Potassium tert-butoxideHCID 23665647—
용매tert-ButanolHCID 6386—
용매TetrahydrofuranHCID 8028—
생성물2,5-Difluoro-4-{1-[4-methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-propoxy}-benzonitrileHCID 5955630995.5%

반응 조건

온도5 °C

반응 단계

To a solution of 900 mg of 1-[4-methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-propan-1-ol in 2 mL of tetrahydrofuran at 5° C. was slowly added 3.3 mL of a molar solution of potassium tert-butoxide in tert-butanol. After stirring at 5° C. for 30 minutes, the resulting solution was slowly added to a solution of 469 mg of 2,4,5-trifluoro-benzonitrile in 2 mL of tetrahydrofuran at −60° C. The resulting mixture was stirred for 1 h at −60° C. then stirred overnight allowing the temperature to warm up to room temperature. It was then poured into water and extracted with dichloromethane. The organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by column chromatography on silica gel (gradient from heptane 100 to heptane 80/ethyl acetate 20) to give 1.25 g of 2,5-difluoro-4-{1-[4-methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-propoxy}-benzonitrile.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07834030B2
출처 데이터셋uspto-grants-2010_11
ORD IDord-640d9a37120e4412a9ff258c71214264
출처 메모uspto-grants-2010_11