참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 2-(Chloromethyl)quinoline | HCID 20394 | — |
| 반응물 | 18-Crown-6 | HCID 28557 | — |
| 반응물 | 6-Hydroxy-2-methyl-2,3-dihydro-1h-inden-1-one | HCID 234338 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 용매 | Hexane | HCID 8058 | — |
| 생성물 | 6-(2-Quinolinylmethoxy)-2-methyl-1-indanone | HCID 19935727 | 84.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05229516 |
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| 출처 데이터셋 | uspto-grants-1993_07 |
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| ORD ID | ord-e8a330f6c75b4e9c96984224ce086cfd |
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| 출처 메모 | uspto-grants-1993_07 |
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