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HRID 986975作成日:2026年10月25日

Tetrabutylammonium Fluoride → 2-(4-Fluorobenzoyl)-3-hydroxypyridine

https://huagongshe.com/reaction/986975

反応式

関与物質

役割名称HCID仕込み量
反応物Tetrabutylammonium FluorideHCID 2724141—
反応物2-(4-Fluorobenzoyl)-3-(tributylsilyloxy)pyridineHCID 22987964—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物2-(4-Fluorobenzoyl)-3-hydroxypyridineHCID 2298797889.6%

反応手順

A solution of 2-(4-fluorobenzoyl)-3-(tributylsilyloxy)pyridine (3.75 g, 11.3 mmol) in tetrahydrofuran (17 ml) was cooled to 0° C. and tetrabutylammonium fluoride (17 ml, 1.0 M in tetrahydrofuran) was added. After 2 h, the reaction mixture was diluted with ethyl acetate. The organic layer was separated, washed with sodium bicarbonate and brine, and dried over sodium sulfate. The organics were removed in vacuo and the residue was purified on a silica gel column using ethyl acetate-hexane (2:8) as the eluant to give 2-(4-fluorobenzoyl)-3-hydroxypyridine (2.2 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06630485B2
出典データセットuspto-grants-2003_10
ORD IDord-81604a4f0516495ca88ab980d1cbf15d
出典メモuspto-grants-2003_10