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HRID 1097437作成日:2026年10月27日

Triethylamine → Ethyl (2E)-3-(1,3,3-trimethyl-2-oxo-2,3-dihydro-1H-indol-7-yl)acrylate

https://huagongshe.com/reaction/1097437

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Ethyl AcrylateHCID 8821—
反応物7-Bromo-1,3,3-trimethylindolin-2-oneHCID 66812879—
触媒HCID 178418397HCID 178418397—
溶媒DimethylformamideHCID 6228—
生成物Ethyl (2E)-3-(1,3,3-trimethyl-2-oxo-2,3-dihydro-1H-indol-7-yl)acrylateHCID 66812761—

反応条件

温度180 °C

反応手順

A mixture of 7-bromo-1,3,3-trimethyl-1,3-dihydro-2H-indol-2-one from Step A (112 mg, 0.44 mmol), ethyl acrylate (0.238 mL, 2.20 mmol), triethylamine (0.124 mL, 0.88 mmol), and (PPh3)4Pd (51 mg, 0.044 mmol) in DMF (1.5 mL) was heated at 180° C. in a microwave reactor for 4 h. The reaction mixture was partitioned between CH2Cl2 (50 mL) and saturated aqueous NaHCO3 (50 mL). The organic layer was washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo. The crude mixture was purified by silica gel chromatography, eluting with a gradient of CH2Cl2:EtOAc—100:0 to 60:40, to give the title compound. MS: m/z=274 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08143266B2
出典データセットuspto-grants-2012_03
ORD IDord-72d7ba4ab98640278a65dd23d81e6c0a
出典メモuspto-grants-2012_03