돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 341493생성일: 2026년 10월 26일

1,4-Difluorobenzene → 1-Benzhydryl-3-(4-fluorophenoxy)azetidine

https://huagongshe.com/reaction/341493

반응식

참여 물질

역할이름HCID투입량
반응물1,4-DifluorobenzeneHCID 10892—
반응물Sodium hydrideHCID 24758—
반응물1-(Diphenylmethyl)azetidin-3-olHCID 330448—
반응물Sodium BicarbonateHCID 516892—
반응물HCID 178418361HCID 178418361—
용매DimethylformamideHCID 6228—
생성물1-Benzhydryl-3-(4-fluorophenoxy)azetidineHCID 1505336967%

반응 단계

To a stirred suspension of sodium hydride (60% dispersion in mineral oil, 0.80 g, 20 mmol) in anhydrous DMF (10 ml) under nitrogen was added dropwise a solution of 1-benzhydryl-azetidin-3-ol (3.5 g, 15 mmol) in DMF (10 ml)—Care: hydrogen gas evolution! The mixture was stirred 30 min after gas evolution had ceased then 1,4-difluorobenzene (1.8 mL, 18 mmol) was added dropwise. The mixture was heated to 100 C and stirred for 12 h, then cooled to room temperature and poured into aq sodium hydrogencarbonate solution (50 ml) and extracted twice with EtOAc (2×50 ml). The combined organic layers were washed with water, concentrated under vacuum and purified by flash column chromatography (25 g silica gel; heptane-EtOAc: 1:0-9:1). The product-containing fractions were combined, concentrated under vacuum, washed with heptane and dried under vacuum to give the title compound (3.256 g, 67%). Method B HPLC-MS: MH+ requires m/z=334 Found: m/z=334, Rt=1.69 min (89%). 1H NMR (250 MHz, CDCl3) δ ppm 7.48-7.39 (4H, m), 7.39-7.12 (6H, m), 6.94 (2H, t), 6.71 (2H, dd), 4.75 (1H, m), 4.46 (1H, s), 3.78-3.65 (2H, m), and 3.20-3.07 (2H, m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08895733B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-100ed274f3804448b70343ad649a3846
출처 메모uspto-grants-2014_11