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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1362500생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1362500

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Potassium CarbonateHCID 11430—
반응물1-(3,4-Difluoro-2-hydroxyphenyl)propan-1-oneHCID 21661595—
용매AcetoneHCID 180—
생성물1-(3,4-Difluoro-2-methoxyphenyl)propan-1-oneHCID 6696948492.1%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07880042B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-3d6334c558d04cea9be8323d1096aee8
출처 메모uspto-grants-2011_02