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2-Nitrophenol → HCID 7434133, 화합물

HRID 1266468
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HRID 1266468 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[OH:10])([O-:3])=[O:2].C(=O)([O-])[O-].[K+].[K+].[Cl:17][C:18]1[CH:19]=[C:20]([CH2:28]Cl)[C:21]2[O:26][CH2:25][O:24][CH2:23][C:22]=2[CH:27]=1>CC(C)=O>[Cl:17][C:18]1[CH:19]=[C:20]([CH2:28][O:10][C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N+:1]([O-:3])=[O:2])[C:21]2[O:26][CH2:25][O:24][CH2:23][C:22]=2[CH:27]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 69472-NitrophenolHCID 11430Potassium CarbonateHCID 27767806-Chloro-8-(chloromethyl)-2,4-dihydro-1,3-benzodioxine

생성물 1

HCID 7434133HCID 7434133, 화합물

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

To a solution of 2-nitrophenol (1.27 g, 9.13 mmol) in acetone (100 mL) was added solid potassium carbonate (1.27 g, 9.13 mmol) followed by 6-chloro-8-(chloromethyl)benzo-1,3-dioxan (1.0 g, 4.57 mmol) and the solution was refluxed for 16 hours. Solvent was evaporated and the residue was purified by column chromatography to give 1-[(6-chloro(2H,4H-benzo[e]1,3-dioxin-8-yl))methoxy]-2-nitrobenzene, a compound of formula (3).

후처리

  1. temperaturethe solution was refluxed for 16 hours
  2. customSolvent was evaporated
  3. customthe residue was purified by column chromatography

출처 및 근거

ORD 기록
ord-2e89f3ac2f3e439cb9fcf3c914b61646
출처 데이터셋
uspto-grants-2003_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06548548B2

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