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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 576091생성일: 2026년 10월 26일

2-Bromo-4'-methylacetophenone → 2-((3-Bromobenzyl)(methyl)amino)-1-p-tolylethanone

https://huagongshe.com/reaction/576091

반응식

참여 물질

역할이름HCID투입량
반응물2-Bromo-4'-methylacetophenoneHCID 69272—
반응물DiisopropylethylamineHCID 81531—
반응물Benzenemethanamine, 3-bromo-N-methyl-HCID 457588—
용매DichloromethaneHCID 6344—
생성물2-((3-Bromobenzyl)(methyl)amino)-1-p-tolylethanoneHCID 6203769198.1%

반응 조건

온도0 °C

반응 단계

To a solution of (3-bromo-benzyl)-methyl-amine (3.0 g, 15.0 mmol) in methylene chloride (60 mL) was added diisopropylethylamine (5.2 mL, 30.0 mmol). The reaction mixture was cooled to 0° C. and treated with 2-bromo-1-p-tolyl-ethanone (3.19 g, 15.0 mmol) portionwise over a period of 10 minutes. The reaction mixture was warmed to room temperature and stirred for 4 hours. The reaction mixture was washed with water (3×), dried over sodium sulfate, filtered, and the solvent was evaporated to afford 2-((3-bromobenzyl)(methyl)amino)-1-p-tolylethanone (4.89 g, 98%) as a viscous, orange oil: 1H NMR (CDCl3, 500 MHz) δ 7.85 (d, J=8.2 Hz, 2H), 7.51 (br s, 1H), 7.38 (d, J=7.9 Hz, 1H), 7.28-7.23 (m, 3H), 7.17 (t, J=7.8 Hz, 1H), 3.78 (s, 2H), 3.63 (s, 2H), 2.41 (s, 3H), 2.35 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09034899B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-5086e6e3f24a40769062a1c9b38f7a48
출처 메모uspto-grants-2015_05