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Potassium Hydroxide → HCID 71467656, 화합물

HRID 922621
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HRID 922621 반응식
[Cl:1][C:2]1[N:3]=[CH:4][NH:5][C:6]=1[Cl:7].[OH-:8].[K+].[Br:10][CH2:11][C:12]1[CH:22]=[CH:21][C:15]([O:16][CH2:17][C:18]([OH:20])=[O:19])=[CH:14][CH:13]=1>C(#N)C>[Br-:10].[C:18]([CH2:17][O:16][C:15]1[CH:21]=[CH:22][C:12]([CH2:11][N:3]2[C:2]([Cl:1])=[C:6]([Cl:7])[N+:5]([CH2:11][C:12]3[CH:22]=[CH:21][C:15]([O:8][CH2:17][C:18]([OH:20])=[O:19])=[CH:14][CH:13]=3)=[CH:4]2)=[CH:13][CH:14]=1)([OH:20])=[O:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 14797Potassium HydroxideHCID 1400184,5-DichloroimidazoleHCID 70106744-(Bromomethyl)phenoxyacetic acid

생성물 1

HCID 71467656HCID 71467656, 화합물

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

4,5-dichloroimidazole (1.00 g, 7.36 mmol) was dissolved in acetonitrile. Potassium hydroxide (0.828 g, 14.72 mmol) was added to the solution and allowed to reflux for 30 min. 2 equivalents of 2-(4-(bromomethyl)phenoxy)acetic acid (3.61 g, 14.72 mmol) was added to the solution and refluxed for 5 h. Solution was filtered to remove the KBr precipitate and neutralized with 6M HBr. Volatiles were removed in vacuo and the resulting white precipitate was collected and analyzed. 1H NMR (300 MHz, DMSO-d6): δ 4.67, 5.51, 7.12, 7.61, 9.23, 12.17.

후처리

  1. temperatureto reflux for 30 min
  2. temperaturerefluxed for 5 h
  3. filtrationSolution was filtered
  4. customto remove the KBr precipitate
  5. customVolatiles were removed in vacuo
  6. customthe resulting white precipitate was collected

출처 및 근거

ORD 기록
ord-d08837c2176a41f78d9eaa9d3086e9eb
출처 데이터셋
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09278951B2

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