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HRID 484242생성일: 2026년 10월 24일

Potassium Carbonate → 6-(2-Quinolinylmethoxy)-2-methyl-1-indanone

https://huagongshe.com/ko/reaction/484242

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2-(Chloromethyl)quinolineHCID 20394—
반응물18-Crown-6HCID 28557—
반응물6-Hydroxy-2-methyl-2,3-dihydro-1h-inden-1-oneHCID 234338—
용매AcetonitrileHCID 6342—
용매HexaneHCID 8058—
생성물6-(2-Quinolinylmethoxy)-2-methyl-1-indanoneHCID 1993572784.8%

반응 단계

A mixture of the phenol (15.16 g, 93.58 mmole) of Step D, powdered anhydrous potassium carbonate (12.93 g, 93.6 mmole), 18-crown-6 (2.47 g, 9.36 mmole) and dry acetonitrile (200 mL) is stirred at room temperature under a nitrogen for 15 minutes. 2-Chloromethylquinoline (free base, freshly prepared from 18.29 g or 102.96 mmole of the hydrochloride salt) is added in one portion and the mixture is placed in an oil bath heated at 65° C. for 11 hours (TLC, dichloromethanemethanol 9:1, UV). The solvent is removed in vacuo and the residue is partitioned between ethyl acetate and water. The organic phase is washed with brine, dried (MgSO4) and evaporated to yield an oil which solidifies upon trituration with hexane (ca. 31 g). The crude product is purified by flash chromatography (on silica Merck-60, absorbed in methylene chloride, eluted with CH2Cl2 -ethyl acetate 90:10 and 85:15) to provide 5.95 g of slightly impure material together with 24.55 g of the pure title compound (pale yellow solid, 84.8%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05229516
출처 데이터셋uspto-grants-1993_07
ORD IDord-e8a330f6c75b4e9c96984224ce086cfd
출처 메모uspto-grants-1993_07