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HRID 1161587作成日:2026年10月24日

Hydrogen Peroxide → 5-Ethoxy-2-fluorophenol

https://huagongshe.com/ja/reaction/1161587

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 SulfiteHCID 24437—
反応物4-FluorophenetoleHCID 68018—
反応物ButyllithiumHCID 178418339—
溶媒Acetic AcidHCID 176—
溶媒TetrahydrofuranHCID 8028—
生成物5-Ethoxy-2-fluorophenolHCID 18003370—

反応手順

To 150 ml of a THF solution containing 10.5 g of 1-ethoxy-4-fluorobenzene, 50 ml of n-butyllithium (1.58 M, hexane solution) was added dropwise at −78° C. under a nitrogen atmosphere. The resulting mixture was stirred for 4 and a half hours, then 8.9 ml of trimethoxy boron was added thereto. Then, the temperature of the mixture was slowly allowed to rise to room temperature. The reaction mixture was stirred for 3 and a half hours, then 12.9 ml of acetic acid and 12.7 ml of a 30% hydrogen peroxide aqueous solution were added thereto at 0° C. The mixture was stirred at room temperature overnight, and then a saturated sodium sulfite aqueous solution was added thereto. The mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine and dried over anhydrous magnesium sulfate. The desiccating agent was removed by filtration, and the filtrate was concentrated under reduced pressure. The residue was crudely purified by silica gel column chromatography (ethyl acetate-heptane) to give a crude product of 5-ethoxy-2-fluorophenol.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07816522B2
出典データセットuspto-grants-2010_10
ORD IDord-6e9c26d66c1f48aa988ae9b63bf1027d
出典メモuspto-grants-2010_10