참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-Bromo-2-Chloroethane | HCID 7849 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | (Quinolin-6-yl)acetonitrile | HCID 21992552 | — |
| 촉매 | Benzyl triethylammonium chloride | HCID 66133 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 1-(Quinolin-6-yl)cyclopropanecarbonitrile | HCID 66812840 | 96% |
반응 단계
60 mL of 50% aqueous NaOH was added to a mixture of 1-bromo-2-chloroethane (22.0 mL, 0.265 mol), quinolin-6-ylacetonitrile (16.0 g, 0.0666 mol), and benzyltriethylammonium chloride (0.99 g, 0.0043 mol) at 50° C. The mixture was stirred at 50° C. for 3 h. After cooling to RT, the reaction mixture was poured into 100 ml of water, and extracted with DCM (3×100 mL). The combined organic layers were dried over anhydrous Na2SO4, filtered through a pad of silica gel and washed with ethyl acetate in DCM (20%). The filtrate was concentrated to give the crude product 1-quinolin-6-ylcyclopropanecarbonitrile (12.4 g, 96%) which was directly used in the next step without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08143251B2 |
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| 출처 데이터셋 | uspto-grants-2012_03 |
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| ORD ID | ord-0a3565002521440ca8d750e627d3c973 |
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| 출처 메모 | uspto-grants-2012_03 |
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