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Methanol → 4-(3-Amino-2-hydroxy-phenyl)-thiophene-2-carboxylic acid hydrobromide

HRID 238716
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 238716
Br.[NH2:2][C:3]1[C:4]([O:17]C)=[C:5]([C:9]2[CH:10]=[C:11]([C:14]([OH:16])=[O:15])[S:12][CH:13]=2)[CH:6]=[CH:7][CH:8]=1.B(Br)(Br)[Br:20].CO>ClCCl>[BrH:20].[NH2:2][C:3]1[C:4]([OH:17])=[C:5]([C:9]2[CH:10]=[C:11]([C:14]([OH:16])=[O:15])[S:12][CH:13]=2)[CH:6]=[CH:7][CH:8]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 887MethanolHCID 25134Boron tribromideHCID 574838484-(3-Amino-2-methoxy-phenyl)-thiophene-2-carboxylic acid hydrobromide

Produkt 1

HCID 574838464-(3-Amino-2-hydroxy-phenyl)-thiophene-2-carboxylic acid hydrobromideAusbeute 17,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

4-(3-Amino-2-methoxy-phenyl)-thiophene-2-carboxylic acid hydrobromide 19b (360 mg, 1.45 mmol) was dissolved in 5 mL of dichloromethane followed by dropwise addition of boron tribromide (2.8 mL, 5.6 mmol). The reaction mixture was reacted at room temperature for 4.5 hours. The reaction mixture was added with 5 mL of methanol and concentrated under reduced pressure. The residue was diluted with 10 mL of ethyl acetate and stirred for 0.5 hours. The mixture was filtered and the filter cake was dried to obtain the title compound 4-(3-amino-2-hydroxy-phenyl)-thiophene-2-carboxylic acid hydrobromide 19c (80 mg, yield 17.5%) as a grey solid.

Aufarbeitung

  1. customThe reaction mixture was reacted at room temperature for 4.5 hours
  2. concentrationconcentrated under reduced pressure
  3. additionThe residue was diluted with 10 mL of ethyl acetate
  4. filtrationThe mixture was filtered
  5. customthe filter cake was dried

Quellen und Nachweise

ORD-Eintrag
ord-ebac0666daf9434a81a06d62d0848ec7
Quelldatensatz
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08642637B2

Notizen zur Reaktion

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