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HRID 234906作成日:2026年10月25日

Ethyl Acetate → (S)-2-ethyl-7-methoxycarbonyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazine

https://huagongshe.com/reaction/234906

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Sodium BicarbonateHCID 516892—
反応物Benzoic acid, 4-amino-3-hydroxy-, methyl esterHCID 7020619—
反応物(R)-2-chlorobutyryl chlorideHCID 7568786—
溶媒WaterHCID 962—
生成物(S)-2-ethyl-7-methoxycarbonyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazineHCID 1063349988.9%

反応手順

To a solution of 2-amino-5-methoxycarbonylphenol [Tetrahedron, 46(15), 5177-5186 (1990)] (7.50 g) in a mixed solvent of ethyl acetate (60 ml) and water (60 ml) were added sodium hydrogen carbonate (5.20 g) and (R)-2-chlorobutyryl chloride (7.50 g) and the mixture was stirred at room temperature for 10 minutes. The organic layer was separated and the solvent was distilled off under reduced pressure. The resulting residue was dissolved in dimethylformamide (90 ml), to the solution was added potassium carbonate (6.20 g) and the mixture was stirred at room temperature overnight. Water was added to the reaction solution and the resulting crystals were taken by filtration to give (S)-2-ethyl-7-methoxycarbonyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazine (9.38 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05597820
出典データセットuspto-grants-1997_01
ORD IDord-b7323edc52714161a112813d18b22f56
出典メモuspto-grants-1997_01