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1-(1H-Imidazol-1-yl)ethanone → 1-Acetyl-3-[4-(ethoxycarbonylmethoxy)benzyl]imidazolium bromide

HRID 1462925
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HRID 1462925 반응식
[C:1]([N:4]1[CH:8]=[CH:7][N:6]=[CH:5]1)(=[O:3])[CH3:2].[Br:9][CH2:10][C:11]1[CH:23]=[CH:22][C:14]([O:15][CH2:16][C:17]([O:19][CH2:20][CH3:21])=[O:18])=[CH:13][CH:12]=1>C(#N)C>[Br-:9].[C:1]([N+:4]1[CH:8]=[CH:7][N:6]([CH2:10][C:11]2[CH:12]=[CH:13][C:14]([O:15][CH2:16][C:17]([O:19][CH2:20][CH3:21])=[O:18])=[CH:22][CH:23]=2)[CH:5]=1)(=[O:3])[CH3:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 171741-(1H-Imidazol-1-yl)ethanoneHCID 12870369Ethyl 2-[4-(bromomethyl)phenoxy]acetate

생성물 1

HCID 1784729941-Acetyl-3-[4-(ethoxycarbonylmethoxy)benzyl]imidazolium bromide수율 98.6%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

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온도
60 °C

실험 절차

2.2 g of 1-acetylimidazole and 5.46 g of ethyl 4-bromomethylphenoxyacetate were added to 5 ml of dry acetonitrile, and the mixture was heated at 60° C. for 2 hours. After completion of the reaction, the solvent was evaporated under reduced pressure. The residue was triturated with an adequate amount of dry diethyl ether and the resulting powder was collected by filtration and dried to obtain 7.5 g of 1-acetyl-3-[4-(ethoxycarbonylmethoxy)benzyl]imidazolium bromide. (98.6% yield). Colorless hygroscopic amorphous.

후처리

  1. customAfter completion of the reaction
  2. customthe solvent was evaporated under reduced pressure
  3. customThe residue was triturated with an adequate amount of dry diethyl ether
  4. filtrationthe resulting powder was collected by filtration
  5. customdried

출처 및 근거

ORD 기록
ord-9f7b7a89136c4505bf9652555cd7e002
출처 데이터셋
uspto-grants-1984_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04461905

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