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HRID 751177作成日:2026年10月27日

4-Pentyn-1-ol → 4-Pentyn-1-ol, 5-[4-(trifluoromethoxy)phenyl]-

https://huagongshe.com/reaction/751177

反応式

関与物質

役割名称HCID仕込み量
反応物4-Pentyn-1-olHCID 79346—
反応物1-Iodo-4-(trifluoromethoxy)benzeneHCID 2777294—
触媒HCID 178418397HCID 178418397—
溶媒PiperidineHCID 8082—
生成物4-Pentyn-1-ol, 5-[4-(trifluoromethoxy)phenyl]-HCID 6882269083%

反応条件

温度50 °C

反応手順

A mixture of 1-iodo-4-trifluoromethoxy-benzene (5 g, 17 mmol), Pd(PPh3)4 (973 mg, 1 mmol) and cuprous iodide (160 mg, 1 mmol) in piperidine (130 ml) was stirred for 30 min at 50° C. under an argon atmosphere. 4-Pentyn-1-ol (2.13 g, 25 mmol) was added within 60 min at 50° C. The temperature was raised to 80° C. and the mixture was stirred for 3 h at this temperature. The reaction mixture was cooled to ambient temperature, poured into a solution of saturated aqueous 10% KHSO4/ice water 1/1 and extracted two times with tert butyl methyl ether. The combined extracts were washed with water and brine (two times) and dried over sodium sulfate. The solvent was removed under reduced pressure and the residue purified by column chromatography (silica gel, heptane/AcOEt) to give 3.4 g (13.9 mmol, 83%) of the title compound as orange oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07405236B2
出典データセットuspto-grants-2008_07
ORD IDord-f6ab7523c228421a8da74e83dd1e4169
出典メモuspto-grants-2008_07