Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 222470생성일: 2026년 10월 26일
N,N,N-trimethyl-1,1-bis(1-methylethoxy)amine → [2-(4-Bromo-5-fluoro-2-nitro-phenyl)-vinyl]-dimethyl-amine
https://huagongshe.com/reaction/222470
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | N,N,N-trimethyl-1,1-bis(1-methylethoxy)amine | HCID 87682 | — |
| 반응물 | 4-Bromo-5-fluoro-2-nitrotoluene | HCID 2779365 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | [2-(4-Bromo-5-fluoro-2-nitro-phenyl)-vinyl]-dimethyl-amine | HCID 73878710 | 83% |
반응 단계
A mixture of N,N-dimethylformamide diisopropyl acetal (1.32 mL, 6.31 mmol) and 1-bromo-2-fluoro-4-methyl-5-nitro-benzene (1.23 g, 5.26 mmol) in dry DMF (15.0 mL) was stirred at 125° C. for 3 h. The resulting mixture was partitioned between EtOAc and water. The organic layer was washed with brine, dried over MgSO4, filtered, and concentrated. The residue was washed with hexane to give [2-(4-bromo-5-fluoro-2-nitro-phenyl)-vinyl]-dimethyl-amine as dark red solid (1.89 mg, 83%). 1H NMR (CDCl3, 400 MHz): 2.92 (s, 6H), 5.88 (d, J=12.3 Hz, 1H), 6.98 (d, J=13.2 Hz, 1H), 7.11 (d, J=10.8 Hz, 1H), 8.10 (d, J=6.9 Hz, 1H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08207216B2 |
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| 출처 데이터셋 | uspto-grants-2012_06 |
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| ORD ID | ord-1b9b703a6db84966ac7373889bb196cb |
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| 출처 메모 | uspto-grants-2012_06 |
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