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HRID 257834作成日:2026年10月25日

Tetrabutylammonium Fluoride → 4-Hydroxy-3-(2-propen-1-yl)benzyl alcohol

https://huagongshe.com/reaction/257834

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4-(Tert-butyldimethylsilyloxy)3-(2-propen-1-yl)benzyl alcoholHCID 54413177—
溶媒TetrahydrofuranHCID 8028—
生成物4-Hydroxy-3-(2-propen-1-yl)benzyl alcoholHCID 53995256793.1%

反応手順

To a solution of approximately 7.26 g (2.6 mmol) of the crude product of Step D, dissolved in 50 mL of anhydrous THF was added 26 mL (2.6 mmol) of tetra-n-butylammonium fluoride and the reaction mixture was stirred at room temperature for 16 hours. The mixture was then evaporated in vacuo and the residual oil was purified on a silica gel flash chromatography column eluted with 5% methanol/chloroform to afford 3.386 g (79%) of the title compound as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05264439
出典データセットuspto-grants-1993_11
ORD IDord-4caddf90da104743a16fe873cebafb5b
出典メモuspto-grants-1993_11