참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | Pyruvic Acid | HCID 1060 | — |
| 반응물 | 4,4'-Dimethoxydiphenylamine | HCID 7571 | — |
| 반응물 | Thionyl Chloride | HCID 24386 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N,N-bis(4-methoxyphenyl)-2-oxopropanamide | HCID 57608129 | 82.4% |
반응 단계
Pyruvic acid (1.00 g, 11.34 mmol) was placed in a 250 mL three-necked round-bottomed flask fitted with a stirring bar, reflux condenser and a nitrogen inlet, and dissolved in 30 mL anhydrous THF at room temperature. Then, SOCl2 (2.03 g, 17.01 mmol) was added dropwise with stirring in 3 hours at room temperature. Bis(4-methoxyphenyl)amine (2.00 g, 8.72 mmol) was added under nitrogen protection. Pyridine (4.14 g, 52.3 mmol) were added to the mixture at 0° C. The reaction mixture was heated to reflux for 12 hours. The reaction was quenched by adding 30 mL of 2N HCl solution. The mixture was extracted with EtOAc (3×20 mL). The organic layers were separated, washed with brine (20 mL) and dried over anhydrous MgSO4. The solvent was removed under reduced pressure to give a yellow residue. The solvent was removed and residue was subjected to flash column chromatography (silica gel, EtOAc/hexanes=3/7 v/v) to give a white solid product, N,N-bis(4-methoxyphenyl)-2-oxopropanamide, 2.15 g, 82.4% yield. MS: m/z 322 [M+Na]+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08637706B2 |
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| 출처 데이터셋 | uspto-grants-2014_01 |
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| ORD ID | ord-f4f649e9303449fcbbd1e04727cd0899 |
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| 출처 메모 | uspto-grants-2014_01 |
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