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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 380490생성일: 2026년 10월 26일

Pyridine → 1-Fluoro-4-(3-iodopropyl)benzene

https://huagongshe.com/reaction/380490

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Lithium iodideHCID 66321—
반응물Methanesulfonic anhydrideHCID 81560—
반응물1-(4-Fluorophenyl)propan-1-olHCID 102470—
용매AcetoneHCID 180—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물1-Fluoro-4-(3-iodopropyl)benzeneHCID 18364840—

반응 단계

To a solution of 2.26 g (14.65 mmol) of 3-(4-fluorophenyl propanol and 3.6 mL (44 mmol) of pyridine in 40 mL of CH2Cl2 at 0° C. was added 5.1 g (29.3 mmol) of methanesulfonic anhydride and the reaction mixture was sitirred for 4 h at rt. The reaction mixture was partitioned between 100 mL of CH2Cl2 and 20 of sat'd NaHCO3 solution. The organic fraction was washed 3 times with sat'd NaHCO3 solution and sat'd NaCl solution, dried over MgSO4 and the filtrate was concentrated several times from heptane to remove pyridine. To the residue in 50 mL of acetone was added 6 g (44 mmol) of LiI and the reaction mixture was Stirred for 20 hr. The reaction mixture was poured into 200 mL of H2O and extracted with ether. The combined organic fractions were washed with sat'd NaCl solution, dried over MgSO4, filtered and the filtrate was concentrated. The residue was purified by chromatography (silica, hexanes: ethyl acetate, 9:1) to give 3.25 g of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06303593B1
출처 데이터셋uspto-grants-2001_10
ORD IDord-c2739e023eb347adba2bb2c9004495eb
출처 메모uspto-grants-2001_10