돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 273735생성일: 2026년 10월 26일

4-Fluoroanisole → (2-Fluoro-5-methoxy-phenyl)-4-pyridylmethanol

https://huagongshe.com/reaction/273735

반응식

참여 물질

역할이름HCID투입량
반응물4-FluoroanisoleHCID 9987—
반응물4-PyridinecarboxaldehydeHCID 13389—
반응물PentamethyldiethylenetriamineHCID 18196—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물(2-Fluoro-5-methoxy-phenyl)-4-pyridylmethanolHCID 15839523—

반응 조건

온도-75 °C

반응 단계

Butyl lithium (47.5 ml of 2.22M solution, 105.6 mmole) was added slowly to a solution of pentamethyldiethylenetriamine (15 ml) and 4-fluoroanisole (12.61 g, 0.1 mole) in THF (150 ml) at -70° C. The solution was stirred for 2 hr at -75° C. and a solution of pyridine-4-aldehyde (9.55 ml, 0.1 mole) in THF was added at -75° C. The mixture was allowed to warm to 25° C. slowly and then quenched with ammonium chloride solution. The mixture was diluted with ethyl acetate and the organic layer was separated. The organic layer was washed with water and 3N hydrochloric acid. The acid washes were then basified with sodium hydroxide and extracted with ether and the ether solution concentrated in vacuo. The crude product was recrystallized from 80% ethanol to give (2-fluoro-5-methoxy-phenyl)-4-pyridylmethanol as a white powder (12.22 g+3.12 g second crop, 65.8% total yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05387593
출처 데이터셋uspto-grants-1995_02
ORD IDord-9e5b4049d4ec4d8581fdf77a8058c374
출처 메모uspto-grants-1995_02