참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 4'-Fluoro-4-methylbiphenyl-3-amine | HCID 46314430 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | [(4'-Fluoro-4-methylbiphenyl-3-yl)amino] (oxo)acetic acid | HCID 66878221 | — |
반응 단계
2.0 g (9.9 mmol) of 4′-fluoro-4-methylbiphenyl-3-amine and 1.64 g (11.9 mmol) of potassium carbonate were suspended in THF, and 1.49 g (10.9 mmol) of chloroglyoxylic acid ethyl were added thereto at 0° C., and stirred at room temperature for 4 hours. After completion of the reaction, ethyl acetate was added to the mixture, and the mixture was washed with an aqueous sodium bicarbonate solution and a sodium chloride solution in this order. The resulting organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure to give 2.76 g of [(4′-fluoro-4-methylbiphenyl-3-yl)amino] (oxo)acetic acid.ethyl ester (yield: 93%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08415479B2 |
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| 출처 데이터셋 | uspto-grants-2013_04 |
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| ORD ID | ord-5096bb7463014ed393a503b841547087 |
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| 출처 메모 | uspto-grants-2013_04 |
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