돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 561418생성일: 2026년 10월 27일

Water → alpha-(4-Fluorophenyl)-4-(trifluoromethyl)benzenemethanol

https://huagongshe.com/reaction/561418

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물1-Bromo-4-fluorobenzeneHCID 9993—
반응물4-(Trifluoromethyl)benzaldehydeHCID 67996—
반응물ButyllithiumHCID 178418339—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물alpha-(4-Fluorophenyl)-4-(trifluoromethyl)benzenemethanolHCID 579773—

반응 단계

1.00 g (5.71 mmol) of 4-bromofluorobenzene were dissolved in 10 ml of tetrahydrofuran at −78° C. Addition of 2.2 ml (6.86 mmol) of a 1.6N solution of n-butyllithium in hexane was followed by stirring for 15 min, and then 1.26 g (6.86 mmol) of trifluoro-p-tolualdehyde dissolved in 10 ml of tetrahydrofuran were added dropwise. The mixture was stirred at −78° C. for 1 h and then at RT for 1 h. The reaction solution was mixed with water and dichloromethane, and the phases were separated. The aqueous phase was extracted with dichloromethane, and the combined organic phases were washed with saturated aqueous sodium chloride solution, dried over sodium sulfate and filtered, and the solvents were removed in vacuo. The crude product was purified by preparative HPLC (mobile phase: acetonitrile-water gradient). 1.02 g (66% of theory) of the title compound were obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08063234B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-747f0697c3b5470eb5ef7c40241ce08a
출처 메모uspto-grants-2011_11