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HRID 548255作成日:2026年10月24日

Acetonitrile → 5-((E)-2-Ethoxycarbonyl-vinyl)-1H-indole-2-carboxylic acid

https://huagongshe.com/ja/reaction/548255

反応式

関与物質

役割名称HCID仕込み量
反応物AcetonitrileHCID 6342—
反応物TriethylamineHCID 8471—
反応物Ethyl AcrylateHCID 8821—
反応物5-Bromo-1H-indole-2-carboxylic acidHCID 252137—
触媒palladium(II) acetateHCID 167845—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物5-((E)-2-Ethoxycarbonyl-vinyl)-1H-indole-2-carboxylic acidHCID 5797164586%

反応手順

5-Bromoindole-2-carboxylic acid (400 mg, 1.66 mmol) and tri-O-tolyl phosphine (96 mg, 0.32 mmol) were added to a microwave tube. Ethyl acrylate (0.56 ml, 5.6 mmol), Et3N (0.92 ml, 6.6 mmol), acetonitrile (2.5 ml) and Pd(OAc)2 (40 mg, 0.18 mmol) were added. The reaction was placed in a CEM microwave at 150 W, 90° C. for 30 minutes with 5 min ramp time. EtOAc was added and the reaction mixture filtered through celite. The celite pad was washed with DCM and the combined organic fractions removed to give a yellow solid. The solid was redissolved in DCM and extracted into saturated sodium hydrogen carbonate. The aqueous layer was washed with DCM and diethyl ether. The aqueous basic layer was acidified with 2M HCl (pH=5) and the product extracted into EtOAc. The solvent was removed to give the required product (370 mg, 86% yield). LCMS purity 86%, m/z 260 [M++H]+

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07939666B2
出典データセットuspto-grants-2011_05
ORD IDord-fd9ad452f293436b86cd1c8eef150f25
出典メモuspto-grants-2011_05