참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Bromide ion | HCID 259 | — |
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | Ethyl 2-oxocyclohexylacetate | HCID 91229 | — |
| 생성물 | Ethyl (2-methylidenecyclohexyl)acetate | HCID 12679490 | 50% |
반응 단계
Triphenylphosphoniummethyl bromide (6.9 g, 19.5 mmol) was added to a suspension of sodium hydride (0.78 g, 60% oil dispersion, 19.5 mmol) (hexane washed) in DMF (50 mL) cooled to 0° C. under a nitrogen atmosphere. The reaction was stirred for 1 h, and then (2-oxo-cyclohexyl)-acetic acid ethyl ester (3.0 g, 16.2 mmol) was added. The reaction was allowed to warm to room temperature and stirred for 18 h. The reaction was partitioned between ethyl acetate and water. The organic layer was washed with brine, dried over magnesium sulfate, and concentrated to give a residue. The product was purified by FCC on silica gel eluting with hexane:ethyl acetate (95:5) to give (2-methylene-cyclohexyl)-acetic acid ethyl ester (1.5 g, 50%) as an oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07125870B2 |
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| 출처 데이터셋 | uspto-grants-2006_10 |
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| ORD ID | ord-110b3519d490411c9150e1774e0cfb28 |
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| 출처 메모 | uspto-grants-2006_10 |
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