홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Methylamine → trans 3-bromo-N-methylcinnamamide

HRID 372482
노트
인쇄 미리보기

반응식

HRID 372482 반응식
[Br:1][C:2]1[CH:3]=[C:4]([CH:10]=[CH:11][CH:12]=1)/[CH:5]=[CH:6]/[C:7](Cl)=[O:8].[CH3:13][NH2:14]>C1C=CC=CC=1>[Br:1][C:2]1[CH:3]=[C:4]([CH:10]=[CH:11][CH:12]=1)/[CH:5]=[CH:6]/[C:7]([NH:14][CH3:13])=[O:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6329MethylamineHCID 14959106trans 3-Bromocinnamoyl chloride

생성물 1

HCID 20327748trans 3-bromo-N-methylcinnamamide

시약·촉매·용매 1

HCID 241Benzene용매

실험 절차

A solution of trans 3-bromocinnamoyl chloride (5 g) in dry benzene (100 ml) was added with stirring to an ethereal (200 ml) solution of methylamine (3 g). After the addition was complete, a slow stream of methylamine gas was bubbled through the reaction mixture at room temperature for one hour. Solvent and excess amine were removed under reduced pressure. The crude product was triturated with water, filtered, and recrystallized from ethanol-water to give trans 3-bromo-N-methylcinnamamide, m.p. 147°-147.5° C. NMR, IR, and elemental analysis were consistent with this structure.

후처리

  1. additionAfter the addition
  2. customa slow stream of methylamine gas was bubbled through the reaction mixture at room temperature for one hour
  3. customSolvent and excess amine were removed under reduced pressure
  4. customThe crude product was triturated with water
  5. filtrationfiltered
  6. customrecrystallized from ethanol-water

출처 및 근거

ORD 기록
ord-ae489c040dda47288ee03333979fc070
출처 데이터셋
uspto-grants-1978_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04091112

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트