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HRID 77326作成日:2026年10月24日

Tetrabutylammonium Fluoride → beta-Methylenephenethyl alcohol

https://huagongshe.com/ja/reaction/77326

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tert-Butyl-dimethyl-(2-phenyl-allyloxy)-silaneHCID 67155247—
溶媒TetrahydrofuranHCID 8028—
生成物beta-Methylenephenethyl alcoholHCID 8010699.8%

反応手順

To a well stirred solution of tert-butyl-dimethyl-(2-phenyl-allyloxy)-silane (1.3 g, 5.23 mmol) in tetrahydrofuran (10 mL) is slowly added a solution of a 1 N tetrabutylammonium fluoride in tetrahydrofuran (10.5 mL, 10.5 mmol). The reaction is allowed to stir for 20 min, quenched by the addition of a saturated aqueous solution of ammonium chloride and extracted several times with ethyl acetate The organic layers are combined, washed with water, brine, dried over magnesium sulfate, filtered and concentrated in vacuo. The residue is purified via silica gel chromatography (10% ethyl acetate in hexanes) to yield 700 mg of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841291B2
出典データセットuspto-grants-2014_09
ORD IDord-040cf4c5b67048c3a151c517cf90500a
出典メモuspto-grants-2014_09