戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2249387作成日:2026年10月25日

Methyl iodide → 1-Bromo-2,4-difluoro-5-methoxybenzene

https://huagongshe.com/reaction/2249387

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Peracetic AcidHCID 6585—
反応物Trimethyl borateHCID 8470—
反応物Potassium CarbonateHCID 11430—
反応物1,5-Dibromo-2,4-difluorobenzeneHCID 10564511—
反応物HCID 178418918HCID 178418918—
溶媒TetrahydrofuranHCID 8028—
生成物1-Bromo-2,4-difluoro-5-methoxybenzeneHCID 6880937923.2%

反応条件

温度0 °C

反応手順

To a solution of 1,3 dibromo-4,6-difluorobenzene (10.0 g, 37 mmol) in THF (50 mL) at −20° C. was added isopropyl magnesium chloride (2.0M in THF, 42 mmol) and the resulting solution warm to 0° C. and stirred for 30 minutes. Trimethylborate (4.7 g, 45 mmol) was added and the mixture stirred at ambient temperature for 1 hour. The solution was recooled to −20° C. and peracetic acid (32%, 50 mmol) was added and the solution was stirred for 30 minutes at ambient temperature. The solution was then quenched with sodium bisulfite (5% solution, 75 mL) and then acidified with 6 N hydrochloric acid and extracted with ethyl ether (2×75 mL). Combined extracts were dried (sodium sulfate) and concentrated. The crude phenol was dissolved in acetonitrile (40 mL) and potassium carbonate (10 g, 74 mmol) and iodomethane (5.7 g, 40 mmol) were added and stirred at ambient temperature for 20 hours. The solution was concentrated and the residue taken into water (50 mL) and extracted with ethyl ether (2×75 mL) and the combined extracts were washed with brine, dried (sodium sulfate), and concentrated. The residue was purified by chromatography (hexanes) to give 1-bromo-2,4-difluoro-5-methoxybenzene (2.0 g, 8.6 mmol): LC/MS (m/z=223).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07314849B2
出典データセットuspto-grants-2008_01
ORD IDord-1e80e3bf6ab845a7a23530927ed62f13
出典メモuspto-grants-2008_01