참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | m-Trifluoromethylphenylacetonitrile | HCID 75360 | — |
| 반응물 | Sodium ethoxide | HCID 2723922 | — |
| 반응물 | Sodium | HCID 5360545 | — |
| 반응물 | Methyl 2-(methylamino)-2-phenylacetate | HCID 13852358 | — |
| 반응물 | Ethanol sodium ethoxide | HCID 23706232 | — |
| 반응물 | HCID 178418361 | HCID 178418361 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | HCID 178481250 | HCID 178481250 | — |
반응 단계
In this example, sodium ethoxide was prepared by mixing 3.0 g of metallic sodium with 100 ml of absolute ethanol. After the evolution of hydrogen stopped, a mixture containing 16.0 g of (3-trifluoromethylphenyl)-acetonitrile and 17.1 g of methyl methylamino-phenylacetate was added dropwise to the sodium ethoxide-ethanol mixture. The resulting mixture was then refluxed overnight (about 16 hours) and then cooled to room temperature. The mixture was then added to 300 ml of water and extracted with diethyl ether. The ethyl ether extract was filtered to remove precipitate. The filtrate was concentrated by evaporation affording a solid. This solid was then triturated in ethyl ether. The ethyl ether was then removed from the solid. The solid was washed several times with ethyl ether and then dried overnight affording 6.2 g of the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04643762 |
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| 출처 데이터셋 | uspto-grants-1987_02 |
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| ORD ID | ord-87c51af8ec874c3ea49862dcb3db61f7 |
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| 출처 메모 | uspto-grants-1987_02 |
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