참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Nitromethane | HCID 6375 | — |
| 반응물 | 1,1,3,3-Tetramethylguanidine | HCID 66460 | — |
| 반응물 | Ethyl 4,4,4-trifluorobut-2-enoate | HCID 141226 | — |
| 용매 | Ethyl Acetoacetate | HCID 8868 | — |
| 생성물 | Ethyl 4,4,4-trifluoro-3-(nitromethyl)butanoate | HCID 268363 | 81% |
반응 단계
1.0 g (5.94 mmol) of 4,4,4-trifluoro-2-butenoic acid ethyl ester and 0.15 mL (1.19 mmol) of 1,1,3,3-tetramethyl guanidine and 1.6 mL (29.8 mmol) of nitromethane were mixed. The resulting mixture was cooled to 0° C. and then stirred for 3 hours at room temperature, followed by addition of 100 mL of ethylacetoacetate. The reaction mixture was washed with water, and then an organic layer was dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to give 1.1 g (4.80 mmol) of the title compound in a yield of 81%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07879848B2 |
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| 출처 데이터셋 | uspto-grants-2011_02 |
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| ORD ID | ord-ebabf3d7f64247c4a01f2fcabda03b19 |
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| 출처 메모 | uspto-grants-2011_02 |
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