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HRID 366708作成日:2026年10月24日

Tetrahydrofuran → 4-Ethynyloxan-4-ol

https://huagongshe.com/ja/reaction/366708

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物Ammonium ChlorideHCID 25517—
反応物Tetrahydro-4H-pyran-4-oneHCID 121599—
反応物HCID 178462451HCID 178462451—
溶媒Diethyl EtherHCID 3283—
生成物4-Ethynyloxan-4-olHCID 15550485—

反応手順

A solution of ethynylmagnesium chloride in THF (0.5 M, 120 mL, 60 mmol) was added with cooling in an ice-water bath to a solution of tetrahydro-4H-pyran-4-one (4.96 g, 50 mmol) (Aldrich) in diethyl ether (300 mL) dropwise over 15 min. The mixture was stirred with cooling for 3 h. Aqueous ammonium chloride solution (100 mL, 15% W/V) was then added and mixture extracted with ether (2×200 mL). The ether layers were washed with saturated aqueous sodium chloride solution (200 mL), then combined, dried (MgSO4), filtered and concentrated to give 4-Ethynyl-tetrahydro-pyran-4-ol as a colorless oil that solidified on standing. (Yield 6.01 g, 96.2%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06130239
出典データセットuspto-grants-2000_10
ORD IDord-07805d1f43314917b75bdcff125bf329
出典メモuspto-grants-2000_10