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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 338420생성일: 2026년 10월 25일

4-Methylmorpholine → 2-(4-bromophenoxy)-N-methylacetamide

https://huagongshe.com/reaction/338420

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물p-Bromophenoxyacetic acidHCID 74657—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물Methylamine hydrochlorideHCID 6364545—
용매DimethylformamideHCID 6228—
생성물2-(4-bromophenoxy)-N-methylacetamideHCID 7535023113.2%

반응 단계

To a solution of (4-bromophenoxy)acetic acid (500 mg, 2.10 mmol) in N,N-dimethylformamide (15 mL) was added methylamine hydrochloride (320 mg, 5.10 mmol), (1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (570 mg, 3.00 mmol), 1-hydroxybenzotriazole (400 mg, 3.00 mmol) and N-methyl-morpholine (600 mg, 6.00 mmol). The mixture was stirred at room temperature overnight. The reaction was quenched with water (20 mL), and then washed three times with ethyl acetate (20 mL). The combined organics was dried and concentrated to give the title compound (580 mg, 90% yield) that was used without further purification. 1H NMR (400 MHz, CDCl3) δ 7.45 (d, 2H), 6.79 (d, 2H), 6.56 (s, 1H), 4.46 (s, 2H), 2.91 (d, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08889730B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-24e449bf88fa4f22b940526ed0d53eca
출처 메모uspto-grants-2014_11