참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | 4-Nitrobenzoyl chloride | HCID 8502 | — |
| 반응물 | Methyl 2-(benzylamino)-2-phenylacetate | HCID 3699844 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | methyl 2-(N-benzyl-4-nitrobenzamido)-2-phenylacetate | HCID 57465368 | 96.4% |
반응 단계
to a solution of methyl 2-(benzylamino)-2-phenylacetate (4.818 g, 18.9 mmol) and pyridine (15.3 ml, 189 mmol) in 75 mL dichloromethane cooled by an ice bath was added 4-nitrobenzoyl chloride (3.50 g, 18.9 mmol) all at once. The cold bath was removed and the reaction stirred to room temperature. The reaction was stirred at room temperature for four hours then concentrated under reduced pressure, taken up in 100 mL heptane and concentrated under reduced pressure. The concentrate was partitioned between 100 mL dichloromethane and 100 mL water. The organic separation was washed with 50 mL brine then stirred over magnesium sulfate, filtered and the filtrate concentrated under reduced pressure to afford a colorless oil. The product was purified by chromatography on silica, eluting with 10-30% ethyl acetate in hexane to afford a colorless foamy solid (7.37 g, 96%). ESI+ m/z=405.1 [MH]+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08404722B2 |
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| 출처 데이터셋 | uspto-grants-2013_03 |
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| ORD ID | ord-b6a573e29af74cc0b7b8e84e531529b8 |
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| 출처 메모 | uspto-grants-2013_03 |
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