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HRID 126719作成日:2026年10月27日

Diethyl Ether → 4-Hydroxy-4-methyl-7-oxo-1-octyne

https://huagongshe.com/reaction/126719

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物Propargyl bromideHCID 7842—
反応物2-Butanone, 4-methoxy-HCID 138889—
反応物MagnesiumHCID 5462224—
反応物HCID 178455849HCID 178455849—
生成物4-Hydroxy-4-methyl-7-oxo-1-octyneHCID 20287598—

反応手順

To a stirred solution of propargylmagnesium bromide in 35 ml. of ether, prepared from 7.65 g. (0.3 moles) of magnesium, 170 mg. of mercuric chloride and 33.6 g. (0.28 moles) of propargyl bromide, is added dropwise under argon atmosphere a solution of 25 g. (0.245 moles) of 4-methoxy-2-butanone [L. R. Fedor, J. Am. Chem. Soc., 91:4, 908 (1969)] in 20 ml. of ether at a rate to maintain gentle refluxing. The resulting mixture is stirred at ambient temperature for an additional 30 minutes then quenched at 5° C. by the addition of 140 ml. of saturated ammonium chloride solution. After filtration the ether phase is separated; the aqueous phase is extracted twice with additional ether. The combined ether extracts are washed with saturated sodium chloride solution, dried with anhydrous magnesium sulfate and taken to dryness in vacuo. Distillation of the residual oil provided 13.7 g. (40%) of product; b.p. 84°-85° C. (13 mm.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04254036
出典データセットuspto-grants-1981_03
ORD IDord-5c760fdfd3744025a9b9928d2d4a4739
出典メモuspto-grants-1981_03