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HRID 380490作成日:2026年10月27日

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

https://huagongshe.com/reaction/380490

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Lithium iodideHCID 66321—
反応物Methanesulfonic anhydrideHCID 81560—
反応物1-(4-Fluorophenyl)propan-1-olHCID 102470—
溶媒AcetoneHCID 180—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物1-Fluoro-4-(3-iodopropyl)benzeneHCID 18364840—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06303593B1
出典データセットuspto-grants-2001_10
ORD IDord-c2739e023eb347adba2bb2c9004495eb
出典メモuspto-grants-2001_10