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HRID 1532832作成日:2026年10月26日

Methyl morpholine oxide → 4-Formyl-2-phenylbenzoyl methionine methyl ester

https://huagongshe.com/reaction/1532832

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl morpholine oxideHCID 82029—
反応物4,4,6-Trimethyl-2-vinyl-1,3,2-dioxaborinaneHCID 107310—
反応物(2-Phenyl4bromobenzoyl)-methionine methyl esterHCID 20622824—
触媒Osmium TetroxideHCID 30318—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
溶媒Sodium CarbonateHCID 10340—
溶媒1,4-Dioxane--water (1/1)HCID 21886435—
生成物4-Formyl-2-phenylbenzoyl methionine methyl esterHCID 10571267—

反応条件

温度25 °C

反応手順

A mixture of (2-phenyl-4-bromobenzoyl) methionine methyl ester (100 mmol), 4,4,6-trimethyl-2-vinyl-1,3,2-dioxaborinane (100 mmol), tetrakis(triphenylphosphine)palladium (0) (3 mmol) in toluene and 2 M sodium carbonate in water (100 mL) is heated at 80° C. until the starting methyl ester disappears. The resulting mixture is extracted with ether, and washed with water, brine, dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. The residue is then purified by column chromatography on silica gel. To a solution of the resulting vinyl compound in dioxane/water (4/1) is added osmium tetraoxide (0.03 equivalent), N-methylmorpholine N-oxide (3 equivalents), and the reaction is stirred at 25° C. until TLC analysis shows the reaction to be complete. The reaction mixture is extracted with ether, which is washed with water and brine, dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. The residue is then purified by column chromatography on silica gel to afford the title product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06204293B1
出典データセットuspto-grants-2001_03
ORD IDord-64d87d992617438cbbffe0767df052a0
出典メモuspto-grants-2001_03