참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Methyloxybenzyl chloride | HCID 69993 | — |
| 반응물 | Cyclopropanecarbonitrile | HCID 79637 | — |
| 반응물 | 1-(4-methoxy-benzyl)-cyclopropanecarbonitrile Sodium bis(trimethylsilyl)amide | HCID 86603547 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-(4-Methoxy-benzyl)-cyclopropanecarbonitrile | HCID 57456950 | — |
반응 단계
1-(4-Methoxy-benzyl)-cyclopropanecarbonitrile Sodium bis(trimethylsilyl)amide (2 M in tetrahydrofuran, 37.5 mL, 75.0 mmol) was slowly added to a solution of cyclopropanecarbonitrile (3.35 g, 49.9 mmol) in THF (30 mL) at room temperature. The reaction mixture was stirred for 20 minutes and then a solution 1-chloromethyl-4-methoxy-benzene (7.83 g, 50.0 mmol) in THF was added. The mixture was heated at reflux for 3 hours and then quenched with a saturated aqueous solution of ammonium chloride (50 mL). The separated aqueous layer was extracted three times with ethyl acetate (50 mL). The combined organic layers were washed with a saturated aqueous solution of sodium bicarbonate and a saturated aqueous solution of sodium chloride, dried over sodium sulfate, filtered, and evaporated to dryness to give crude 1-(4-methoxy-benzyl)-cyclopropanecarbonitrile, which was used directly in the next step.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08541453B2 |
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| 출처 데이터셋 | uspto-grants-2013_09 |
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| ORD ID | ord-fbc156986c084e01b76995a2830ab6c6 |
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| 출처 메모 | uspto-grants-2013_09 |
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