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HRID 237861作成日:2026年10月27日

Iodoethane → Methyl acetate hexane

https://huagongshe.com/reaction/237861

反応式

関与物質

役割名称HCID仕込み量
反応物IodoethaneHCID 6340—
反応物Sodium hydrideHCID 24758—
反応物4-(Tetrahydro-pyran-2-yloxy)-but-2-yn-1-olHCID 11123315—
溶媒DimethylformamideHCID 6228—
生成物Methyl acetate hexaneHCID 234493021%
生成物2-(4-Ethoxy-but-2-ynyloxy)-tetrahydro-pyranHCID 68529463—

反応条件

温度0 °C

反応手順

An oven dried 500 ml RBF was charged with NaH (60% in mineral oil) (1.41 g, 35.3 mmol) and suspended in DMF (100 mL). The mixture was cooled to 0° C. and 4-(tetrahydro-pyran-2-yloxy)-but-2-yn-1-ol (prepared in accordance with the procedures of Tamaru et al., Bull. Chem. Soc. Jpn., 1995, 1689-1705) (6.0 g, 35.3 mmol) was added. The reaction mixture was allowed to reach room temperature and stirred for one hour. To the mixture was added iodoethane (20.8 g, 133 mmol). The reaction mixture was stirred for 3.5 hours at room temperature before being quenched with ice/H2O and extracted with MeOAc. The organic phase was washed with brine, dried (Na2SO4) and concentrated. Silica gel chromatography (1-20% MeOAc/hexane) provided 4.71 g of 2-(4-ethoxy-but-2-ynyloxy)-tetrahydro-pyran as a clear oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08642603B2
出典データセットuspto-grants-2014_02
ORD IDord-fd436759d4e74f2f98770a0ccab266a0
出典メモuspto-grants-2014_02