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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 61883생성일: 2026년 10월 24일

Ethyl Acetate → tert-Butyl 6-cyano-2-(2-(4-ethyl-3-iodophenyl)propan-2-yl)benzofuran-3-carboxylate

https://huagongshe.com/ko/reaction/61883

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Cesium carbonateHCID 10796—
반응물Benzonitrile, 4-chloro-3-nitro-HCID 13655—
반응물tert-butyl 4-(4-ethyl-3-iodophenyl)-4-methyl-3-oxopentanoateHCID 66834434—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물tert-Butyl 6-cyano-2-(2-(4-ethyl-3-iodophenyl)propan-2-yl)benzofuran-3-carboxylateHCID 6683500426%

반응 단계

4-(4-Ethyl-3-iodo-phenyl)-4-methyl-3-oxo-pentanoic acid tert-butyl ester (1.00 g, 2.40 mmol) was dissolved in NMP (4 ml), added with cesium carbonate (1.56 g, 4.80 mmol, 2.0 eq.), and the mixture was stirred for 5 min. The NMP solution (2 ml) of 4-chloro-3-nitro-benzonitrile (542 mg, 2.88 mmol, 1.2 eq.) was added thereto, and the mixture was stirred at 50° C. for 64 hrs under nitrogen atmosphere. After cooling to room temperature, ethyl acetate (20 ml) was added and the organic layer was washed with saturated aqueous solution of ammonium chloride (20 ml). The organic layer was further washed with saturated brine and dried over sodium sulfate. The drying agent was removed by filtration and the residues obtained after concentration under reduced pressure were purified by silica gel column chromatography (ethyl acetate/hexane) to obtain the title compound (white amorphous, 320 mg, 26%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440922B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-4e5a2c03260648c7a8a120668540e2ae
출처 메모uspto-grants-2016_09