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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 548255생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물TriethylamineHCID 8471—
반응물Ethyl AcrylateHCID 8821—
반응물5-Bromo-1H-indole-2-carboxylic acidHCID 252137—
촉매palladium(II) acetateHCID 167845—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물5-((E)-2-Ethoxycarbonyl-vinyl)-1H-indole-2-carboxylic acidHCID 5797164586%

반응 단계

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]+

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07939666B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-fd9ad452f293436b86cd1c8eef150f25
출처 메모uspto-grants-2011_05