돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 963409생성일: 2026년 10월 26일

Water → Cyclopropanecarboxylic acid acetyl-(3-iodo-phenyl)-amide

https://huagongshe.com/reaction/963409

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Cyclopropanecarbonyl chlorideHCID 77637—
반응물3'-IodoacetanilideHCID 87971—
촉매Hydrochloric AcidHCID 313—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물Cyclopropanecarboxylic acid acetyl-(3-iodo-phenyl)-amideHCID 5445254592%

반응 단계

In analogy to Example 13ap), from N-benzyl-5-bromo-isatin (G.Tacconi et al., J. Prakt. Chem. 315, 339 (1973)) there is obtained the corresponding N-benzyl-5-bromo-isatin oxime as a yellow solid. Yield: 94%. Mass spectrum: peaks inter alia at 330 (M+, 17%); 285 (14%), 91 (100%). 13ar) 1.36 g of N-acetyl-3-iodo-aniline are dissolved in 25 ml of methylene chloride and treated with 61 mg of 4-dimethylamino-pyridine. A solution of 5.25 ml of cyclopropanecarbonyl chloride in 7 ml of methylene chloride is added dropwise to this solution. The mixture is stirred at room temperature overnight, then poured into 100 ml of water and made weakly acid with a few drops of dil. hydrochloric acid. Extraction with ethyl acetate and chromatography on silica gel with ethyl acetate gives 1.85 g of cyclopropanecarboxylic acid acetyl-(3-iodo-phenyl)-amide as a yellowish oil which solidifies in time. Yield: 92%. Mass spectrum: peaks inter alia at 329 (M+, 8%); 287 (58%), 69 (100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05763450
출처 데이터셋uspto-grants-1998_06
ORD IDord-c6787882c2154b19abdf5fc4d08a98d8
출처 메모uspto-grants-1998_06