Water → 2-Cyclopropanecarbonyl-7-methoxybenzofuran-4-carboxylic Acid 4-nitrophenyl Ester

HRID 1108311Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1108311
[CH:1]1([C:4]([C:6]2[O:7][C:8]3[C:9](=[C:11]([C:17]([OH:19])=[O:18])[CH:12]=[CH:13][C:14]=3[O:15][CH3:16])[CH:10]=2)=[O:5])[CH2:3][CH2:2]1.[N+:20]([C:23]1[CH:28]=[CH:27][C:26](O)=[CH:25][CH:24]=1)([O-:22])=[O:21].Cl.CN(C)CCCN=C=NCC.O>ClCCl.CN(C)C1C=CN=CC=1>[N+:20]([C:23]1[CH:28]=[CH:27][C:26]([O:18][C:17]([C:11]2[CH:12]=[CH:13][C:14]([O:15][CH3:16])=[C:8]3[O:7][C:6]([C:4]([CH:1]4[CH2:2][CH2:3]4)=[O:5])=[CH:10][C:9]=23)=[O:19])=[CH:25][CH:24]=1)([O-:22])=[O:21]

Komponenten

7

Versuchsvorschrift

To a stirred suspension of 2-cyclopropanecarbonyl-7-methoxybenzofuran-4-carboxylic acid (0.50 g) in dichloromethane (30 ml) under an atmosphere of nitrogen was added 4-nitrophenol (0.29 g), 4-dimethylaminopyridine (20 mg) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.41 g). The reaction mixture was stirred at room temperature for 18 h. Water (30 ml) was added and the mixture extracted with dichloromethane (150 ml). The organic layer was separated, dried over magnesium sulfate, filtered and concentrated in vacuo. Purification by flash chromatography on silica eluting with 40% ethyl acetate in hexane afforded the title compound as a pale yellow solid (0.59 g).

Aufarbeitung

  1. extractionthe mixture extracted with dichloromethane (150 ml)
  2. customThe organic layer was separated
  3. dry with materialdried over magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo
  6. customPurification by flash chromatography on silica eluting with 40% ethyl acetate in hexane

Quellen und Nachweise

ORD-Eintrag
ord-0ffbe286285745c8822697759a08e46d
Quelldatensatz
uspto-grants-2000_05
Patentnummer
US06066657

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