참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2,4-Dichlorobenzylamine | HCID 1485 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 2-Bromo-1-(3-nitrophenyl)ethan-1-one | HCID 75213 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-(2,4-Dichlorobenzylamino)-1-(3-nitrophenyl)ethanone | HCID 67460064 | — |
반응 단계
Into a 250-mL 3-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed a solution of 2-bromo-1-(3-nitrophenyl)ethanone (10.0 g, 41.15 mmol, 1.00 equiv) in THF (150 mL), (2,4-dichlorophenyl)methanamine (7.16 g, 40.91 mmol, 1.00 equiv) and triethylamine (5.96 g, 59.01 mmol, 1.50 equiv). The resulting solution was stirred for 2 h at 25° C. The solids were filtered out. The filtrate was concentrated to dryness and used for next step, assuming theoretical yield.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08541448B2 |
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| 출처 데이터셋 | uspto-grants-2013_09 |
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| ORD ID | ord-4a1ec25d65af442db55f85cba8b5dbc7 |
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| 출처 메모 | uspto-grants-2013_09 |
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