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Sodium Hydroxide → 5-bromo-3-(3-methoxypropoxy)-1H-pyridin-2-one

HRID 252363
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HRID 252363 반응식
[OH-].[Na+].[Br:3][C:4]1[CH:5]=[C:6]([OH:11])[C:7](=[O:10])[NH:8][CH:9]=1.I[CH2:13][CH2:14][CH2:15][O:16][CH3:17]>C(O)(=O)C>[Br:3][C:4]1[CH:5]=[C:6]([O:11][CH2:13][CH2:14][CH2:15][O:16][CH3:17])[C:7](=[O:10])[NH:8][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 14798Sodium HydroxideHCID 125630835-Bromopyridine-2,3-diolHCID 135229891-Iodo-3-methoxypropane

생성물 1

HCID 231494755-bromo-3-(3-methoxypropoxy)-1H-pyridin-2-one

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

To a 1.4M NaOH solution at 0° C. are added 0.9 mol 5-bromo-3-hydroxy-1H-pyridin-2-one [34206-49-0]. The mixture is allowed to stir for 15 minutes and 0.9 mmol 1-iodo-3-methoxypropane [61542-10-7] are added carefully at 0° C. The mixture is stirred at room temperature for 3 hours, then neutralized with acetic acid to pH 7. The mixture is extracted with chloroform (10×) and the organic layer is dried over sodium sulphate, filtered and concentrated. The title compound is obtained from the residue by means of flash chromatography (SiO2 60F) and identified based on its Rf value.

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후처리

  1. stirringThe mixture is stirred at room temperature for 3 hours
  2. extractionThe mixture is extracted with chloroform (10×)
  3. dry with materialthe organic layer is dried over sodium sulphate
  4. filtrationfiltered
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-906cddcac298485ea485c8f0b863acf3
출처 데이터셋
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07868036B2

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