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HRID 1362500作成日:2026年10月25日

Methyl iodide → 1-(3,4-Difluoro-2-methoxyphenyl)propan-1-one

https://huagongshe.com/reaction/1362500

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物Potassium CarbonateHCID 11430—
反応物1-(3,4-Difluoro-2-hydroxyphenyl)propan-1-oneHCID 21661595—
溶媒AcetoneHCID 180—
生成物1-(3,4-Difluoro-2-methoxyphenyl)propan-1-oneHCID 6696948492.1%

反応手順

30.1 g (161 mmol) of 2,3-difluorophenyl propionate in 16 ml of 1,2-dichlorobenzene are added dropwise to 21.5 g (161 mmol) of aluminum trichloride in 16 ml of 1,2-dichlorobenzene and the mixture is subsequently stirred at 100° C. for 6 hours. It is cooled, diluted with dichloromethane and poured cautiously onto a mixture of 2 M hydrochloric acid and ice. The phases are separated, extraction is carried out with dichloromethane and the extracts are washed with saturated sodium chloride solution and dried over sodium sulphate. The crude product is purified by column chromatography on silica gel (hexane/ethyl acetate 10-20%) to give 21.5 g of 1-(3,4-difluoro-2-hydroxyphenyl)propan-1-one. 21.4 g (115 mmol) of 1-(3,4-difluoro-2-hydroxyphenyl)propan-1-one are dissolved in 170 ml of acetone, and the solution is admixed with 29.5 g of potassium carbonate and 13 ml (209 mmol) of methyl iodide. The mixture is boiled under reflux for 4 hours and stirred at room temperature for 12 hours and then the solvent is largely removed. The residue is poured into water and subjected to extraction with diethyl ether. The extracts are washed with water, dried over sodium sulphate and, following the removal of the solvent in vacuo, give 21.2 g of 1-(3,4-difluoro-2-methoxyphenyl)propan-1-one.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07880042B2
出典データセットuspto-grants-2011_02
ORD IDord-3d6334c558d04cea9be8323d1096aee8
出典メモuspto-grants-2011_02