Potassium Carbonate → 6-(2-Quinolinylmethoxy)-2-methyl-1-indanone

HRID 484242

Reaktionsgleichung

Reaktionsgleichung von HRID 484242
[OH:1][C:2]1[CH:10]=[C:9]2[C:5]([CH2:6][CH:7]([CH3:12])[C:8]2=[O:11])=[CH:4][CH:3]=1.C(=O)([O-])[O-].[K+].[K+].C1OCCOCCOCCOCCOCCOC1.Cl[CH2:38][C:39]1[CH:48]=[CH:47][C:46]2[C:41](=[CH:42][CH:43]=[CH:44][CH:45]=2)[N:40]=1>CCCCCC.C(#N)C>[N:40]1[C:41]2[C:46](=[CH:45][CH:44]=[CH:43][CH:42]=2)[CH:47]=[CH:48][C:39]=1[CH2:38][O:1][C:2]1[CH:10]=[C:9]2[C:5]([CH2:6][CH:7]([CH3:12])[C:8]2=[O:11])=[CH:4][CH:3]=1

Komponenten

7

Edukt 4

HCID 11430Potassium CarbonateHCID 203942-(Chloromethyl)quinolineHCID 2855718-Crown-6HCID 2343386-Hydroxy-2-methyl-2,3-dihydro-1h-inden-1-one

Produkt 1

HCID 199357276-(2-Quinolinylmethoxy)-2-methyl-1-indanoneAusbeute 84,8 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6342AcetonitrileLösungsmittelHCID 8058HexaneLösungsmittel

Versuchsvorschrift

A mixture of the phenol (15.16 g, 93.58 mmole) of Step D, powdered anhydrous potassium carbonate (12.93 g, 93.6 mmole), 18-crown-6 (2.47 g, 9.36 mmole) and dry acetonitrile (200 mL) is stirred at room temperature under a nitrogen for 15 minutes. 2-Chloromethylquinoline (free base, freshly prepared from 18.29 g or 102.96 mmole of the hydrochloride salt) is added in one portion and the mixture is placed in an oil bath heated at 65° C. for 11 hours (TLC, dichloromethanemethanol 9:1, UV). The solvent is removed in vacuo and the residue is partitioned between ethyl acetate and water. The organic phase is washed with brine, dried (MgSO4) and evaporated to yield an oil which solidifies upon trituration with hexane (ca. 31 g). The crude product is purified by flash chromatography (on silica Merck-60, absorbed in methylene chloride, eluted with CH2Cl2 -ethyl acetate 90:10 and 85:15) to provide 5.95 g of slightly impure material together with 24.55 g of the pure title compound (pale yellow solid, 84.8%).

Aufarbeitung

  1. additionis added in one portion
  2. customthe mixture is placed in an oil bath
  3. temperatureheated at 65° C. for 11 hours (TLC, dichloromethanemethanol 9:1, UV)
  4. customThe solvent is removed in vacuo
  5. customthe residue is partitioned between ethyl acetate and water
  6. washThe organic phase is washed with brine
  7. dry with materialdried (MgSO4)
  8. customevaporated
  9. customto yield an oil which
  10. customThe crude product is purified by flash chromatography (on silica Merck-60, absorbed in methylene chloride, eluted with CH2Cl2 -ethyl acetate 90:10 and 85:15)

Quellen und Nachweise

ORD-Eintrag
ord-e8a330f6c75b4e9c96984224ce086cfd
Quelldatensatz
uspto-grants-1993_07
Patentnummer
US05229516

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