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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 482245생성일: 2026년 10월 24일

Benzyl Bromide → 3-Benzyloxy-6,7-dimethoxy-quinoline

https://huagongshe.com/ko/reaction/482245

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물Sodium hydrideHCID 24758—
반응물2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
반응물6,7-Dimethoxyquinolin-3-olHCID 10058766—
용매TetrahydrofuranHCID 8028—
생성물3-Benzyloxy-6,7-dimethoxy-quinolineHCID 10085863—

반응 단계

To 3-hydroxy-6,7-dimethoxyquinoline (150 mg; 0.73 mmol) in 3 mL THF is added benzyl bromide (0.13 mL; 188 mg; 1.10 mmol) and NaH (59 mg; 1.46 mmol). This is stirred at room temperature for 1 hour and 25 mg of NaH added followed by 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)pyrimidinone (DMPU) (255 mg; 2.07 mmol) and stirred at room temperature for 31/2 hours. The reaction mixture is partitioned between EtOAc and distilled H2O and extracted 2× with EtOAc. The latter is washed with brine, dried (MgSO4), filtered, evaporated to dryness and chromatographed with 1% MeOH/CHCl3 to obtain 3-benzyloxy-6,7-dimethoxyquinoline m.p. 146.5°-148.5° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05795889
출처 데이터셋uspto-grants-1998_08
ORD IDord-5edbacb9a58941fc899bdf83916ca751
출처 메모uspto-grants-1998_08