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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 598447생성일: 2026년 10월 24일

Methylamine → N-methyl-3-(4-nitrophenoxy)benzamide

https://huagongshe.com/ko/reaction/598447

반응식

참여 물질

역할이름HCID투입량
반응물MethylamineHCID 6329—
반응물3-(4-Nitrophenoxy)benzoic acidHCID 767919—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
촉매Ni methylmorpholineHCID 131728719—
용매DichloromethaneHCID 6344—
생성물N-methyl-3-(4-nitrophenoxy)benzamideHCID 2361456948.2%

반응 단계

A mixture of 4-(3-carboxyphenoxy)-1-nitrobenzene (3.72 g, 14.4 mmol), EDCI.HCl (3.63 g, 18.6 mmol), Ni-methylmorpholine (1.6 mL, 14.5 mmol) and methylamine (2.0 M in THF 8 mL, 16 mmol) in CH2Cl2 (45 mL) was stirred at room temp. for 3 d, then concentrated under reduced pressure. The residue was dissolved in EtOAc (50 mL) and the resulting mixture was extracted with a 1M HCl solution (50 mL). The aqueous layer was back-extracted with EtOAc (2×50 mL). The combined organic phases were washed with a saturated NaCl solution (50 mL), dried (Na2SO4), and concentrated under reduced pressure to give 4-(3-(N-methylcarbamoyl)phenoxy)-1-nitrobenzene as an oil (1.89 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07897623B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-4378fea5add54ce29dfdc319cee76cd5
출처 메모uspto-grants-2011_03