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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1190015생성일: 2026년 10월 25일

Bromobenzene → 5-Cyclohex-1-enyl-3-phenylamino-thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/1190015

반응식

참여 물질

역할이름HCID투입량
반응물BromobenzeneHCID 7961—
반응물Cesium carbonateHCID 10796—
반응물Binap, (A+-)-HCID 634876—
반응물5-Cyclohex-1-enyl-3-aminothiophene-2-carboxylic acid methyl esterHCID 57795401—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매DichloromethaneHCID 6344—
용매1,4-DioxaneHCID 31275—
생성물5-Cyclohex-1-enyl-3-phenylamino-thiophene-2-carboxylic acid methyl esterHCID 5779536076%

반응 단계

To a solution of 5-cyclohex-1-enyl-3-amino-thiophene-2-carboxylic acid methyl ester (111 mg, 0.47 mmol) and bromobenzene (54 μL, 0.51 mmol) in dry dioxane (3 mL) were added cesium carbonate (459 mg, 1.41 mmol) and Pd2 dba3 (43 mg, 0.047 mmol), and the mixture was deoxygenated by bubbling nitrogen through solution for 10 min. Then BINAP (47 mg, 0.075 mmol) was added to the mixture, and it was refluxed under nitrogen overnight. The mixture was diluted with CH2Cl2 and filtered through celite washing with CH2Cl2. Filtrate was concentrated under reduced pressure and purified by column chromatography on silica gel eluting with 2-30% EtOAc in hexanes to give 111 mg (76%) of 5-cyclohex-1-enyl-3-phenylamino-thiophene-2-carboxylic acid methyl ester.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08674118B2
출처 데이터셋uspto-grants-2014_03
ORD IDord-5ac8cb038f854bc383aa1ffc32dff29d
출처 메모uspto-grants-2014_03