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HRID 547987作成日:2026年10月26日

tert-Butyl hydroperoxide → 1H-Indene-2-carboxylic acid, 5-chloro-2,3-dihydro-2-hydroxy-1-oxo-, methyl ester

https://huagongshe.com/reaction/547987

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyl hydroperoxideHCID 6410—
反応物1H-Indene-2-carboxylic acid, 5-chloro-2,3-dihydro-1-oxo-, methyl esterHCID 11042391—
触媒Zirconium(4+) propan-2-olateHCID 3083750—
溶媒TolueneHCID 1140—
溶媒AcetonitrileHCID 6342—
生成物1H-Indene-2-carboxylic acid, 5-chloro-2,3-dihydro-2-hydroxy-1-oxo-, methyl esterHCID 1097758589%

反応条件

温度30 °C

反応手順

To a solution of methyl 5-chloro-2,3-dihydro-1-oxo-1H-indene-2-carboxylate (also known as methyl 5-chloro-1-oxo-2,3-dihydroindene-2-carboxylate) (0.500 g, 2.23 mmol) (Formula IIa wherein R1 is OCH3 and R4 is Cl) and zirconium(1V) isopropoxide (0.0086 g, 0.022 mmol) in toluene (1.34 g, 1.56 mL) at 30° C. was added an aqueous solution of tert-butyl hydroperoxide (70%, 0.316 g, 2.46 mmol). The reaction mixture was stirred for 24 hours at 30° C. and then diluted with acetonitrile (about 6 mL). Quantitative HPLC analysis showed 92% conversion of methyl 5-chloro-2,3-dihydro-1-oxo-1H-indene-2-carboxylate, forming racemic methyl 5-chloro-2,3-dihydro-2-hydroxy-1-oxo-1H-indene-2-carboxylate in 89% yield (97% chemoselectivity).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07939685B2
出典データセットuspto-grants-2011_05
ORD IDord-4932bb66191d4e22ae50ef1098387465
出典メモuspto-grants-2011_05