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HRID 341664作成日:2026年10月26日

2-Methyl-3-butyn-2-ol → HCID 59445912、化合物

https://huagongshe.com/reaction/341664

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methyl-3-butyn-2-olHCID 8258—
反応物MethoxyacetoneHCID 22172—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 59445912HCID 5944591229%

反応条件

温度-78 °C

反応手順

A solution of 2-methyl-3-butyne-2-ol (25 g, 0.3 mol) in tetrahydrofuran (250 ml) is cooled to −78° C. under a nitrogen atmosphere and to this solution, n-butyl lithium (1.6 molar solution in hexanes, 372 ml, 0.59 mol) is added slowly over 1.5-2.0 hours. The reaction mixture is stirred for 1 hour at −78° C. and a solution of methoxyacetone (38 g, 0.43 mol) in tetrahydrofuran (50 ml) is added. The reaction mixture is stirred at −78° C. for one hour, allowed to come to ambient temperature, and stirred for 2-3 hours. The reaction mixture is cooled to 10° C. and quenched with ice cold water. The mixture is extracted with ethyl acetate (3×250 ml), and the organic phases are combined, washed with water, and dried over anhydrous sodium sulfate. The mixture is filtered, and the filtrate is evaporated under reduced pressure. The residue is purified by column chromatography on silica gel to give 1-methoxy-2,5-dimethylhex-3-yne-2,5-diol (15 g) as a colourless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08895761B2
出典データセットuspto-grants-2014_11
ORD IDord-ea1b2174633e4a91bae731d3e8590d84
出典メモuspto-grants-2014_11