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HRID 1644583作成日:2026年10月27日

Tributylphosphine → Methyl 3-isopropoxy-5-(3-pyridin-3-ylpropoxy)benzoate

https://huagongshe.com/reaction/1644583

反応式

関与物質

役割名称HCID仕込み量
反応物TributylphosphineHCID 13831—
反応物3-PyridinepropanolHCID 17861—
反応物1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
反応物Methyl 3-hydroxy-5-isopropoxybenzoateHCID 23072925—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物Methyl 3-isopropoxy-5-(3-pyridin-3-ylpropoxy)benzoateHCID 6677569886.2%

反応手順

To a solution (60 ml) of methyl 5-hydroxy-3-isopropoxybenzoate (2.0 g) and 3-(pyridin-3-yl)propanol (1.6 g) in THF were added successively 1,1′-(azodicarbonyl)dipiperidine (2.9 g) and tributylphosphine (2.8 ml) under ice-cooling, and the mixture was stirred overnight at room temperature. n-Hexane (100 ml) was added to the reaction mixture, and the precipitated crystals were removed by filtration. The filtrate was concentrated under reduced pressure, and the residue was purified by column chromatography (LL, Biotage cartridge, ethyl acetate:n-hexane=15:85→1:4) to give methyl 3-isopropoxy-5-(3-pyridin-3-ylpropoxy)benzoate (2.70 g, 86%) as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08124617B2
出典データセットuspto-grants-2012_02
ORD IDord-1567ed6032804ef2a8faf4a7aa64cbdf
出典メモuspto-grants-2012_02