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HRID 1093394作成日:2026年10月27日

Propargyl alcohol → 3-(5-Methyl-2-thienyl)-2-propyne-1-ol

https://huagongshe.com/reaction/1093394

反応式

関与物質

役割名称HCID仕込み量
反応物Propargyl alcoholHCID 7859—
反応物TriphenylphosphineHCID 11776—
反応物DiisopropylethylamineHCID 81531—
反応物2-Iodo-5-methylthiopheneHCID 140096—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒Palladium, tris[mu-[(1,2-eta:4,5-eta)-(1E,4E)-1,5-diphenyl-1,4-pentadien-3-one]]di-, compd. with trichloromethane (1:1)HCID 11029508—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物3-(5-Methyl-2-thienyl)-2-propyne-1-olHCID 59407516—

反応手順

A mixture of 2-iodo-5-methylthiophene (5.00 g), copper(I) iodide (82 mg), triphenylphosphine (286 mg), tris(dibenzylideneacetone)dipalladium(0) chloroform adduct (445 mg), propargyl alcohol (1.91 ml), diisopropylethylamine (15.1 ml) and tetrahydrofuran (30 ml) was stirred at room temperature for 20 hr. The reaction mixture was added to water, and the mixture was extracted with ethyl acetate, washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=3:1-2:1) to give the object product (1.48 g) as a brown oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08129361B2
出典データセットuspto-grants-2012_03
ORD IDord-39f77001690a4a04b01060a72968ea12
出典メモuspto-grants-2012_03