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Hydrochloric Acid → 4-(5-Phenyl-pentanoylamino)-thiophene-3-carboxylic acid

HRID 14594
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 14594
C[O:2][C:3]([C:5]1[C:9]([NH:10][C:11](=[O:22])[CH2:12][CH2:13][CH2:14][CH2:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)=[CH:8][S:7][CH:6]=1)=[O:4].[Li+].[OH-].Cl>O1CCCC1.CO>[C:16]1([CH2:15][CH2:14][CH2:13][CH2:12][C:11]([NH:10][C:9]2[C:5]([C:3]([OH:4])=[O:2])=[CH:6][S:7][CH:8]=2)=[O:22])[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 313Hydrochloric AcidHCID 3939Lithium HydroxideHCID 686887754-(5-Phenyl-pentanoylamino)-thiophene-3-carboxylic acid methyl ester

Produkt 1

HCID 160680444-(5-Phenyl-pentanoylamino)-thiophene-3-carboxylic acidAusbeute 43,7 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 21899815MeOH tetrahydrofuranLösungsmittel

Versuchsvorschrift

To a solution of 4-(5-phenyl-pentanoylamino)-thiophene-3-carboxylic acid methyl ester (50 mg, 0.16 mmol) in tetrahydrofuran/methanol 2/1 (1.5 ml) was added a 1 N aqueous LiOH solution (0.95 ml, 0.95 mmol). The reaction mixture was stirred at room temperature for 2 h, acidified with 1 N HCl and extracted two times with ethyl acetate. The combined organic layers were washed with water and brine and dried over sodium sulfate. The solvent was removed under reduced pressure and the crude product was purified by thin layer chromatography (SiO2, dichloromethane) to give the title compound as colorless oil (20 mg, 0.07 mmol, 42%).

Aufarbeitung

  1. extractionextracted two times with ethyl acetate
  2. washThe combined organic layers were washed with water and brine
  3. dry with materialdried over sodium sulfate
  4. customThe solvent was removed under reduced pressure
  5. customthe crude product was purified by thin layer chromatography (SiO2, dichloromethane)

Quellen und Nachweise

ORD-Eintrag
ord-bcbdfeb5c2c8411faccfa2cce2abe3a4
Quelldatensatz
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07732452B2

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