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HRID 411142作成日:2026年10月25日

Tributylphosphine → HCID 21867689、化合物

https://huagongshe.com/reaction/411142

反応式

関与物質

役割名称HCID仕込み量
反応物TributylphosphineHCID 13831—
反応物3,4-DimethoxyphenolHCID 16251—
反応物1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
反応物4-(1-Hydroxy-3-butenyl)benzonitrileHCID 11019345—
溶媒TolueneHCID 1140—
生成物HCID 21867689HCID 2186768968.6%

反応手順

A cooled (0° C.) mixture of 4-(1-hydroxy-3-butenyl)benzonitrile (14.6 g, 84.3 mmol) and 3,4-dimethoxyphenol (19.5 g, 125.4 mmol) in toluene (500 mL) was treated with tributylphosphine (32.14 mL of 97% purity, 25.6 g, 126.4 mmol), followed by 1,1′-(azodicarbonyl)dipiperidine (31.8 g, 126.4 mmol). After addition was complete, the reaction mixture thickened and the temperature rose to 15° C. Additional toluene was added (500 mL), and the mixture stirred at rt overnight. The precipitate of tributylphosphine oxide was then removed by filtration and the filtrate concentrated in vacuo to give 65.8 g of crude product. This was purified by chromatography on silica gel, eluting with toluene:methanol (98:2), to yield 17.9 g of the sub-title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06559143B1
出典データセットuspto-grants-2003_05
ORD IDord-88a33979ca2345679982399a6e5a2de6
出典メモuspto-grants-2003_05