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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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1-Methylimidazole → 1-Propenyl-3-methylimidazolium Bromide

HRID 47943
노트
인쇄 미리보기

반응식

HRID 47943 반응식
[Br:1][CH2:2][CH2:3][CH3:4].[CH3:5][N:6]1[CH:10]=[CH:9][N:8]=[CH:7]1>>[Br-:1].[CH3:5][N+:6]1[CH:10]=[CH:9][N:8]([CH2:2][CH2:3][CH3:4])[CH:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 13901-MethylimidazoleHCID 78401-Bromopropane

생성물 1

HCID 111600281-Propenyl-3-methylimidazolium Bromide수율 94.9%

반응 조건

온도
70 °C

실험 절차

450 g of 1-bromopropane (3.66 mol) are loaded into a 1 l glass reactor. The mixture is heated to 70° C. and then 200 g of 1-methylimidazole (2.44 mol) are poured in dropwise, with stirring. The mixture is left to react for 1 h at 70° C. After returning to room temperature, the mixture is separated by decantation. The bottom ionic liquid phase is recovered, washed with toluene (1×100 ml), and then evaporated under vacuum. 475 g of 1-methyl-3-propylimidazolium bromide are obtained in the form of a yellow liquid. The product is used as a base without further purification.

후처리

  1. waitThe mixture is left
  2. customto react for 1 h at 70° C
  3. customAfter returning to room temperature
  4. customthe mixture is separated by decantation
  5. customThe bottom ionic liquid phase is recovered
  6. washwashed with toluene (1×100 ml)
  7. customevaporated under vacuum

출처 및 근거

ORD 기록
ord-422262e1a46e466d8c83a2b55dd26e5f
출처 데이터셋
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06700007B2

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