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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 718358생성일: 2026년 10월 24일

2,4,5-Trifluorophenylacetic acid → 2-(2,4,5-Trifluorophenyl)ethan-1-ol

https://huagongshe.com/ko/reaction/718358

반응식

참여 물질

역할이름HCID투입량
반응물2,4,5-Trifluorophenylacetic acidHCID 2777950—
반응물Aluminium lithium hydrideHCID 21226445—
용매TetrahydrofuranHCID 8028—
생성물2-(2,4,5-Trifluorophenyl)ethan-1-olHCID 1775083992%

반응 단계

A solution of 2-(2,4,5-trifluorophenyl)acetic acid (1 g, 5.26 mmol) in dry THF (20 mL) was carefully added over 2 min to solution of 2M LAH (10.52 mL, 10.52 mmol) at 0° C. The reaction mixture was allowed to warm to rt and was stirred for 6 h. The reaction was quenched with 0.5 mL of water (stir for 10 min), 0.5 mL of 15% NaOH/water (stir for 10 min), and then 1.0 mL of water. After stirring for 18 h, the mixture was filtered through celite. The filtrate was concentrated in vacuum. The residue was dried under high vacuum for 16 h to afford 2-(2,4,5-trifluorophenyl)ethanol (850 mg, 4.83 mmol, 92% yield) as a clear viscous oil, which was used as is in the next step without further purification. 1H NMR (500 MHz, CDCl3) δ 7.11 (ddd, J=10.3, 8.7, 7.2 Hz, 1H), 6.93 (td, J=9.7, 6.6 Hz, 1H), 3.87 (t, J=6.5 Hz, 2H), 2.88 (t, J=6.5 Hz, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09193720B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-f0a353c24d1b4510a32efe4af3ee6e52
출처 메모uspto-grants-2015_11