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HRID 640490作成日:2026年10月23日

Propargyl bromide → 4-[(2-Propynyloxy)methyl]benzyl alcohol

https://huagongshe.com/ja/reaction/640490

反応式

関与物質

役割名称HCID仕込み量
反応物Propargyl bromideHCID 7842—
反応物TetrahydrofuranHCID 8028—
反応物1,4-BenzenedimethanolHCID 11506—
反応物Sodium hydrideHCID 24758—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物4-[(2-Propynyloxy)methyl]benzyl alcoholHCID 5452013158%

反応手順

To a mixture of sodium hydride (400 mg, 8.4 mmol, 50% in oil) and tetrahydrofuran (30 mL) was added 1,4-benzenedimethanol (2.3 g, 17 mmol) at 0° C., and then N,N-dimethylformamide (30 mL) was added. The reaction mixture was stirred at room temperature for 10 minutes, after which propargyl bromide (1.0 g, 8.4 mmol) was added dropwise to the reaction mixture at 0° C. The reaction mixture was stirred at room temperature for 1 hour, after which water was added to the reaction mixture, which was extracted with ethyl acetate. The organic layer was washed and saturated aqueous sodium chloride, and was concentrated under a reduced pressure. The residue thus obtained was purified by NH silica gel column chromatography (heptane:ethyl acetate=3:2) to obtain the title compound (860 mg, 58%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07691882B2
出典データセットuspto-grants-2010_04
ORD IDord-069a5b2d59254c22abe480ca278edf54
出典メモuspto-grants-2010_04