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Imidazole → HCID 18467051, Verbindung

HRID 2229251
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2229251
O[CH2:2][CH2:3][CH2:4][C:5]([C:7]1[CH:16]=[CH:15][C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[CH:8]=1)=[O:6].C(N(CC)CC)C.CS(Cl)(=O)=O.[NH:29]1[CH:33]=[CH:32][N:31]=[CH:30]1>C1COCC1.[Na+].[I-].O>[N:29]1([CH2:2][CH2:3][CH2:4][C:5]([C:7]2[CH:16]=[CH:15][C:14]3[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=3)[CH:8]=2)=[O:6])[CH:33]=[CH:32][N:31]=[CH:30]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 4

HCID 795ImidazoleHCID 8471TriethylamineHCID 31297Methanesulfonyl chlorideHCID 184670444-Hydroxy-1-(2-naphthyl)-1-butanone

Produkt 1

HCID 18467051HCID 18467051, VerbindungAusbeute 22,7 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 5238
Sodium Iodide
Katalysator
HCID 962WaterLösungsmittel
HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

To a cooled (0° C.) solution of 4-hydroxy-1-(2-naphthyl)-1-butanone (4.32 g) in THF (60 ml) were added triethylamine (5.6 ml) and methanesulfonyl chloride (2.4 ml) successively. The mixture was stirred at 0° for 1 hour. Imidazole (2.93 g) and NaI (0.02 g) were added to the mixture and resulting mixture was refluxed for 16 hours. Water was added and the mixture was concentrated. The residue was extracted with ethyl acetate and the extract was washed with water and brine, dried and concentrated. The residue was chromatographed on silica gel, eluting with ethyl acetate-methanol=20:1, followed by crystallization from ethyl acetate-CH2Cl2-cyclohexane to give the titled compound (1.21 g) as a colorless solid.

Aufarbeitung

  1. customresulting mixture
  2. temperaturewas refluxed for 16 hours
  3. concentrationthe mixture was concentrated
  4. extractionThe residue was extracted with ethyl acetate
  5. washthe extract was washed with water and brine
  6. customdried
  7. concentrationconcentrated
  8. customThe residue was chromatographed on silica gel
  9. washeluting with ethyl acetate-methanol=20:1
  10. customfollowed by crystallization from ethyl acetate-CH2Cl2-cyclohexane

Quellen und Nachweise

ORD-Eintrag
ord-8de3ba9fd7164ab49ee731895bf7df1e
Quelldatensatz
uspto-grants-2002_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06420375B1

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