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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Tetrahydrofuran → 3,3',3''-(benzene-1,3,5-triyltris(methylene))tris(4,5-dichloro-1-(naphthalen-1-ylmethyl)-1H-imidazol-3-ium) bromide

HRID 922692
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HRID 922692 반응식
[Cl:1][C:2]1[N:3]=[CH:4][NH:5][C:6]=1[Cl:7].[OH-].[K+].[Br:10][CH2:11][C:12]1[CH:17]=[C:16]([CH2:18]Br)[CH:15]=[C:14]([CH2:20]Br)[CH:13]=1.[Br:22][CH2:23][C:24]1[C:33]2[C:28](=[CH:29][CH:30]=[CH:31][CH:32]=2)[CH:27]=[CH:26][CH:25]=1.[CH2:34]1[CH2:38]O[CH2:36][CH2:35]1>>[Br-:10].[C:16]1([CH2:18][N+:3]2[C:2]([Cl:1])=[C:6]([Cl:7])[N:5]([CH2:38][C:34]3[C:33]4[C:24](=[CH:25][CH:26]=[CH:27][CH:28]=4)[CH:23]=[CH:36][CH:35]=3)[CH:4]=2)[CH:17]=[C:12]([CH2:11][N+:3]2[C:2]([Cl:1])=[C:6]([Cl:7])[N:5]([CH2:23][C:24]3[C:33]4[C:28](=[CH:29][CH:30]=[CH:31][CH:32]=4)[CH:27]=[CH:26][CH:25]=3)[CH:4]=2)[CH:13]=[C:14]([CH2:20][N+:3]2[C:2]([Cl:1])=[C:6]([Cl:7])[N:5]([CH2:36][C:35]3[C:31]4[C:34](=[CH:35][CH:36]=[CH:29][CH:30]=4)[CH:38]=[CH:38][CH:34]=3)[CH:4]=2)[CH:15]=1.[Br-:22].[Br-:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 5

HCID 8028TetrahydrofuranHCID 14797Potassium HydroxideHCID 1378441-(Bromomethyl)naphthaleneHCID 1400184,5-DichloroimidazoleHCID 5302581,3,5-Tris(bromomethyl)benzene

생성물 1

HCID 867197463,3',3''-(benzene-1,3,5-triyltris(methylene))tris(4,5-dichloro-1-(naphthalen-1-ylmethyl)-1H-imidazol-3-ium) bromide

실험 절차

4,5-dichloroimidazole (3.00 g, 21.90 mmol) was dissolved in THF and brought to reflux. Potassium hydroxide (2.46 g, 43.80 mmol) was added to the solution and allowed to reflux for 30 min. 1,3,5-tris(bromomethyl)benzene (2.61, 7.30 mmol) was added to the solution and refluxed overnight. Solution was filtered while hot to remove the KBr precipitate and the filtrate returned to reflux. 1-(bromomethyl)naphthalene (4.84 g, 21.90 mmol) was added to the solution and refluxed for 3 h. The volatiles were removed in vacuo and the resulting waxy yellow solid was washed in ethyl ether. A resulting product will be collected and analyzed.

후처리

  1. temperatureto reflux
  2. temperatureto reflux for 30 min
  3. temperaturerefluxed overnight
  4. filtrationSolution was filtered while hot
  5. customto remove the KBr precipitate
  6. temperatureto reflux
  7. temperaturerefluxed for 3 h
  8. customThe volatiles were removed in vacuo
  9. washthe resulting waxy yellow solid was washed in ethyl ether
  10. customA resulting product will be collected

출처 및 근거

ORD 기록
ord-a82ad7559bce4983b97eac21cd1f30bb
출처 데이터셋
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09278951B2

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