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HRID 222339作成日:2026年10月25日

Hydrogen Peroxide → 3-Fluoro-2-(trifluoromethyl)phenol

https://huagongshe.com/reaction/222339

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen PeroxideHCID 784—
反応物Trimethyl borateHCID 8470—
反応物Sodium HydroxideHCID 14798—
反応物2-Bromo-6-fluorobenzotrifluorideHCID 2773345—
反応物LithiumHCID 3028194—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物3-Fluoro-2-(trifluoromethyl)phenolHCID 2497198240%

反応手順

A solution of 3-fluoro-2-(trifluoromethyl)bromobenzene (1 g, 4.1 mmol) in tetrahydrofuran (25 mL) was added dropwise to nbutyl lithium (2.5M in hexanes, 3.2 mL, 8 mmol), at −78° C., and the mixture was stirred at this temperature for 30 minutes. Trimethyl borate (1.84 mL, 16.4 mmol) was added and the reaction mixture was stirred at −78° C. for a further 30 minutes and at room temperature for 18 hours. 2M sodium hydroxide solution (4 mL) and 35% hydrogen peroxide solution (2 mL) were then added and the mixture was heated under reflux for 3 hours. The reaction mixture was cooled to room temperature and diluted with diethyl ether (100 mL). The aqueous layer was separated and the organic solution was washed with 2M sodium hydroxide solution. The combined basic washings were acidified with 2M hydrochloric acid, extracted with diethyl ether (2×50 mL) and the organic solution was concentrated in vacuo to afford the title compound as a yellow oil in 40% yield, 300 mg. 1H NMR (400 MHz, CD3OD) δ: 6.64 (m, 1H), 6.75 (d, 1H), 7.36 (q, 1H)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08207198B2
出典データセットuspto-grants-2012_06
ORD IDord-4163f46eeefb46d8bc31f4ed23d3bbf9
出典メモuspto-grants-2012_06