Hydrochloric Acid → 4-chloro-1-(4-methoxybutyl)-2-phenyl-1H-imidazole-5-carboxylic acid

HRID 1184213Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1184213
[Cl:1][C:2]1[N:3]=[C:4]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[N:5]([CH2:9][CH2:10][CH2:11][CH2:12][O:13][CH3:14])[C:6]=1[CH:7]=[O:8].Cl([O-])=[O:22].[Na+].P([O-])(O)(O)=O.[Na+].Cl>C(O)(C)(C)C.CC(=CC)C>[Cl:1][C:2]1[N:3]=[C:4]([C:15]2[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=2)[N:5]([CH2:9][CH2:10][CH2:11][CH2:12][O:13][CH3:14])[C:6]=1[C:7]([OH:22])=[O:8]

Komponenten

7

Edukt 4

HCID 313Hydrochloric AcidHCID 23668197Sodium ChloriteHCID 23672064Monosodium phosphateHCID 583555004-chloro-1-(4-methoxybutyl)-2-phenyl-1H-imidazole-5-carbaldehyde

Produkt 1

HCID 583555054-chloro-1-(4-methoxybutyl)-2-phenyl-1H-imidazole-5-carboxylic acidAusbeute 87,6 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6386tert-ButanolLösungsmittelHCID 105532-Methyl-2-buteneLösungsmittel

Versuchsvorschrift

To a solution of 4-chloro-1-(4-methoxybutyl)-2-phenyl-1H-imidazole-5-carbaldehyde (790 mg) in tert-butanol (15 ml) and 2-methyl-2-butene (1.5 ml) was added aqueous solution (4 ml) of sodium chlorite (300 mg) and sodium dihydrogen phosphate (400 mg), and the mixture was stirred at room temperature for 12 hr. 1M Hydrochloric acid was added, and the mixture was adjusted to pH 3, and extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give the object product (730 mg).

Aufarbeitung

  1. extractionextracted with ethyl acetate
  2. washThe extract was washed with saturated brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customThe solvent was evaporated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-9586d79f214041f29ca991880f68e9b6
Quelldatensatz
uspto-grants-2014_03
Patentnummer
US08664380B2

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