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HRID 1392374作成日:2026年10月25日

Potassium Carbonate → (R)-2-Hydroxy-N-(4-nitrophenethyl)-2-phenylacetamide

https://huagongshe.com/reaction/1392374

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物(-)-Mandelic acidHCID 11914—
反応物4-NitrophenethylamineHCID 95153—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物HCID 178418300HCID 178418300—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物(R)-2-Hydroxy-N-(4-nitrophenethyl)-2-phenylacetamideHCID 5967838087.8%

反応手順

To a mixture of 9.77 g of 4-nitrophenylethylamine 1/2 sulfate, 6.00 g of (R)-mandelic acid, 4.70 g of potassium carbonate and 60 mL of N,N-dimethylformamide, 6.14 g of hydroxybenztriazole and 8.70 g of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide monohydrochloride (EDC) were added, and the mixture was stirred at around room temperature for 2 hours. 0.87 g of EDC was further added, and the mixture was stirred at around room temperature overnight. The reaction solution was diluted with water and extracted with ethyl acetate. The organic layer was washed successively with 1M hydrochloric acid aqueous solution, 20% potassium carbonate aqueous solution and water, and then concentrated in vacuo. The residue was recrystallized from toluene to obtain 10.4 g of (R)-2-hydroxy-N-[2-(4-nitrophenyl)ethyl]-2-phenylacetamide as a pale yellow crystal.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07342117B2
出典データセットuspto-grants-2008_03
ORD IDord-82177b2151ae4cee9791adcbcaa740f2
出典メモuspto-grants-2008_03