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Potassium Iodide → 1-(4-chlorobutyl)-4-methylpyridin-2(1H)-one

HRID 2421919
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HRID 2421919 반응식
[OH:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][N:3]=1.C(=O)([O-])[O-].[K+].[K+].Br[CH2:16][CH2:17][CH2:18][CH2:19][Cl:20].[I-].[K+]>CO.O>[Cl:20][CH2:19][CH2:18][CH2:17][CH2:16][N:3]1[CH:4]=[CH:5][C:6]([CH3:8])=[CH:7][C:2]1=[O:1]
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참가 물질

7

반응물 4

HCID 4875Potassium IodideHCID 11430Potassium CarbonateHCID 813641-Bromo-4-chlorobutaneHCID 178428601HCID 178428601, 화합물

생성물 1

HCID 592346451-(4-chlorobutyl)-4-methylpyridin-2(1H)-one수율 72.8%

시약·촉매·용매 2

HCID 887Methanol용매
HCID 962
Water
용매

실험 절차

A mixture of 2-hydroxy-4-methylpyridine (1.50 g, 13.75 mmol) and potassium carbonate (1.90 g, 13.75 mmol) in 13 ml of methanol were stirred at room temperature for 15 minutes and then 1-bromo-4-chlorobutane (3.54 g, 20.62 mmol) and a spatula tip of potassium iodide were added thereto. The reaction mixture was heated to reflux for 6 hours and then stirred at room temperature for 12 hours. Water was then added to the reaction mixture, and the aqueous mixture was extracted with dichloromethane. Drying of the organic phase and removal of the desiccant by filtration was followed by concentration of the organic phase in vacuo. Flash chromatography of resulting residue on silica gel (eluent: CH2Cl2/CH3OH: 98:2) afforded 2.0 g of 1-(4-chlorobutyl)-4-methylpyridin-2(1H)-one.

후처리

  1. temperatureThe reaction mixture was heated
  2. temperatureto reflux for 6 hours
  3. stirringstirred at room temperature for 12 hours
  4. extractionthe aqueous mixture was extracted with dichloromethane
  5. customDrying of the organic phase and removal of the
  6. filtrationdesiccant by filtration

출처 및 근거

ORD 기록
ord-f327b21ea8044f0899ad237ca1a2f34e
출처 데이터셋
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07960386B2

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