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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 593266생성일: 2026년 10월 24일

Benzoyl chloride → N-(1-methyl-3-oxo-indan-5-yl)benzamide

https://huagongshe.com/ko/reaction/593266

반응식

참여 물질

역할이름HCID투입량
반응물Benzoyl chlorideHCID 7412—
반응물TriethylamineHCID 8471—
반응물Ethyl AcetateHCID 8857—
반응물3-methyl-6-nitro-2,3-dihydro-1H-inden-1-oneHCID 600702—
용매DichloromethaneHCID 6344—
생성물N-(1-methyl-3-oxo-indan-5-yl)benzamideHCID 8670333787.7%

반응 단계

As presented in the following reaction formula, a solution of benzoyl chloride (PhCOCl; 6.7 g, 0.043 mol) in dichloromethane (DCM; 20 mL) was added at 0° C. to a mixture of 3-methyl-6-nitro-2,3-dihydro-1-H-inden-1-one (7 g, 0.043 mol) and triethylamine (9.6 g, 0.095 mol) in dichloromethane (DCM; 100 mL), and the reaction mixture was stirred for 2 hours. After the completion of reaction, the mixture was washed with water (50 mL), saturated sodium hydrogen carbonate (50 mL) and saturated brine (50 mL) and then concentrated to give a crude product. The crude product was purified by silica gel (50 g) column chromatography (product of Merck Co., Ltd.) using an eluent of pentane (PE):ethyl acetate (10:1 (by volume)) to give the desired product N-(1-methyl-3-oxo-indan-5-yl)benzamide (10 g, yield: 87%) as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09242928B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-5feabcee308f439686424084a76a7a3a
출처 메모uspto-grants-2016_01