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HRID 2111055作成日:2026年10月27日

Vinyl propanoate → 4-Hydroxy-2-vinyloxyphenyl phenyl ketone

https://huagongshe.com/reaction/2111055

反応式

関与物質

役割名称HCID仕込み量
反応物Vinyl propanoateHCID 7750—
反応物2,4-DihydroxybenzophenoneHCID 8572—
反応物Sodium CarbonateHCID 10340—
反応物[4-(Ethenyloxy)-2-hydroxyphenyl](phenyl)methanoneHCID 22935772—
溶媒TolueneHCID 1140—
生成物4-Hydroxy-2-vinyloxyphenyl phenyl ketoneHCID 22935793—

反応条件

温度100 °C

反応手順

To a mixture of di-μ-chlorobis(1,5-cyclooctadiene)diiridium(I) [Ir(cod)Cl]2 (1.27 g, 1.9 mmol) and sodium carbonate (24.9 g, 0.23 mol)) in toluene (280 ml) were added 2,4-dihydroxybenzophenone (40 g, 0.19 mol) and vinyl propionate (75.1 g, 0.75 mo1), followed by stirring at 100° C. in an atmosphere of argon gas for 3 hours. The reaction mixture was analyzed by gas chromatography to find that 2-hydroxy-4-vinyloxyphenyl phenyl ketone [i.e., 2-hydroxy-4-vinyloxyphenyl(phenyl)methanone] and 4-hydroxy-2-vinyloxyphenyl phenyl ketone [i.e., 4-hydroxy-2-vinyloxyphenyl(phenyl)methanone] were formed in yields of 90% and 2%, respectively, with a conversion from 2,4-dihydroxybenzophenone of 99%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07518021B2
出典データセットuspto-grants-2009_04
ORD IDord-48382192c150440e846d4792ba50ccb8
出典メモuspto-grants-2009_04