참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Fluoride | HCID 522689 | — |
| 반응물 | Thiophene-3-boronic acid | HCID 581760 | — |
| 반응물 | Trifluoromethanesulfonic acid 2,2,4-trimethyl-1,2-dihydroquinolin-6-yl ester | HCID 20760320 | — |
| 촉매 | palladium(II) acetate | HCID 167845 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2,2,4-Trimethyl-6-thiophen-3-yl-1,2-dihydroquinoline | HCID 22566532 | 32.1% |
반응 단계
To a dry 50 mL round bottom flask charged with a mixture of trifluoromethanesulfonic acid 2,2,4-trimethyl-1,2-dihydroquinolin-6-yl ester (0.50 g, 1.56 mmol), Pd(OAc)2 (0.035 g, 0.156 mmol), di-tert-butylbiphenylphosphine (DTBBPP) (0.093 g, 0.312 mmol), and KF (0.27 g, 4.67 mmol) suspended in THF (5 mL), was added 3-thiopheneboronic acid (0.30 g, 2.33 mmol). The flask was evacuated and flushed three times with argon and the reaction mixture was allowed to stir at room temperature for 2 days. The reaction mixture was filtered through diatomaceous earth and diluted with EtOAc (50 mL). The mixture was sequentially washed with water (10 mL), NaOH (1.0 M, 10 mL), and brine (10 mL). The organic phase was dried over sodium sulfate (Na2SO4), filtered, and concentrated in vacuo. The crude residue was purified by chromatography (silica gel, 30% dichloromethane in hexanes) to give 2,2,4-trimethyl-6-thiophen-3-yl-1,2-dihydroquinoline (0.128 g, 32%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06858627B2 |
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| 출처 데이터셋 | uspto-grants-2005_02 |
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| ORD ID | ord-a5b4cd99bc954d7a8d729932cf755d5b |
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| 출처 메모 | uspto-grants-2005_02 |
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