Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1795599생성일: 2026년 10월 27일
Cesium carbonate → 4-(5,8,8-Trimethyl-7,8-dihydro-naphthalen-2-yl-amino)-benzoic acid ethyl ester
https://huagongshe.com/reaction/1795599
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Cesium carbonate | HCID 10796 | — |
| 반응물 | Ethyl 4-bromobenzoate | HCID 22043 | — |
| 반응물 | Bis(diphenylphosphino)-1,1'-binaphthyl | HCID 18630801 | — |
| 반응물 | 5,8,8-Trimethyl-7,8-dihydro-naphthalen-2-ylamine | HCID 22218345 | — |
| 촉매 | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 4-(5,8,8-Trimethyl-7,8-dihydro-naphthalen-2-yl-amino)-benzoic acid ethyl ester | HCID 21024367 | — |
반응 단계
General Procedure L To a solution of 5,8,8-trimethyl-7,8-dihydro-naphthalen-2-yl-amine (Compound 64, 0.33 g, 1.8 mmol) and ethyl 4-bromobenzoate (0.52 g, 2.3 mmol) in 10.0 mL of toluene while stirring under argon were added cesium carbonate (0.89 g, 2.7 mmol), tris(dibenzylideneacetone)dipalladium(0) (Pd2(dba)3, 33 mg, 0.04 mmol) and bis(diphenylphosphino)-1,1′-binaphthyl (BINAP, 47 mg, 0.08 mmol) consecutively. The reaction was then heated at 100° C. for 24 h. The reaction was then cooled to room temperature, diluted with water and extracted 2 times with ethyl ether. The combined organic extracts were washed with brine, dried over MgSO4, filtered, and the solvents were removed in vacuo. The crude product was purified by silica gel chromatography (10% ethyl acetate in hexanes) to give the title compound as a yellow solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07026487B2 |
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| 출처 데이터셋 | uspto-grants-2006_04 |
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| ORD ID | ord-079a93512d444eb4a575adc250df4e07 |
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| 출처 메모 | uspto-grants-2006_04 |
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