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HRID 26269作成日:2026年10月27日

Hydrochloric Acid → 2-Methyl-1-phenoxybut-3-yn-2-ol

https://huagongshe.com/reaction/26269

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Diethyl EtherHCID 3283—
反応物1-Phenoxy-2-propanoneHCID 69313—
反応物(Triethylsilyl)acetyleneHCID 637947—
反応物ButyllithiumHCID 178418339—
生成物2-Methyl-1-phenoxybut-3-yn-2-olHCID 23266458—

反応手順

To 3.1 parts of triethylsilylacetylene in 15 parts by volume of ether at -30° C. is added 8 parts by volume of 2.5 molar n-butyl lithium. The reaction mixture is allowed to come to room temperature and 3 parts of phenoxyacetone in 5 parts by volume of ether is added. The reaction mixture is stirred at room temperature for one hour and then poured into ether and dilute (1 N) hydrochloric acid solution. The ether layer is washed with water and dried over anhydrous sodium sulfate. The solvents are removed at reduced pressure and the residual oil is dissolved in 15 parts by volume of dimethylformamide containing about 5 parts of powdered potassium fluoride. The reaction mixture is stirred at 70°-80° C. for about 1 hour. The reaction mixture is worked up by diluting with ether and washing several times with water. The ether layer is dried over anhydrous sodium sulfate and stripped of solvent under reduced pressure. The residual oil is isolated by low pressure liquid chromatography on silica gel using 30% ethyl acetate/hexane as eluent to provide 3-hydroxy-3-methyl-4-phenoxy-1-butyne.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04149006
出典データセットuspto-grants-1979_04
ORD IDord-d431de35d5a549f68ce722f17aad84d3
出典メモuspto-grants-1979_04