돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25796생성일: 2026년 10월 24일

Potassium Fluoride → 2,2,4-Trimethyl-6-thiophen-3-yl-1,2-dihydroquinoline

https://huagongshe.com/ko/reaction/25796

반응식

참여 물질

역할이름HCID투입량
반응물Potassium FluorideHCID 522689—
반응물Thiophene-3-boronic acidHCID 581760—
반응물Trifluoromethanesulfonic acid 2,2,4-trimethyl-1,2-dihydroquinolin-6-yl esterHCID 20760320—
촉매palladium(II) acetateHCID 167845—
용매TetrahydrofuranHCID 8028—
생성물2,2,4-Trimethyl-6-thiophen-3-yl-1,2-dihydroquinolineHCID 2256653232.1%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858627B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-a5b4cd99bc954d7a8d729932cf755d5b
출처 메모uspto-grants-2005_02