Ethanol → C-(6-Phenoxy-benzofuran-2-yl)-methylamine

HRID 1171211Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1171211
C(O)C.[O:4]([C:11]1[CH:31]=[CH:30][C:14]2[CH:15]=[C:16]([CH2:18][N:19]3C(=O)C4C(=CC=CC=4)C3=O)[O:17][C:13]=2[CH:12]=1)[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1.O.NN>O>[O:4]([C:11]1[CH:31]=[CH:30][C:14]2[CH:15]=[C:16]([CH2:18][NH2:19])[O:17][C:13]=2[CH:12]=1)[C:5]1[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=1

Komponenten

5

Edukt 3

HCID 702EthanolHCID 24654Hydrazine hydrate (1:1)HCID 576082842-(6-Phenoxy-benzofuran-2-ylmethyl)-isoindole-1,3-dione

Produkt 1

HCID 57608283C-(6-Phenoxy-benzofuran-2-yl)-methylamineAusbeute 68 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

To an ethanol (5 mL) solution of 2-(6-phenoxy-benzofuran-2-ylmethyl)-isoindole-1,3-dione (209 mg, 566 μmol) described in Production Example 49-1-3 was added hydrazine hydrate (549 μL, 11.3 mmol) at room temperature, which was stirred for 1 hour while heating under reflux. Water was added to the reaction solution at room temperature followed by extraction with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated under a reduced pressure and the residue was purified by silica gel column chromatography (ethyl acetate:methanol=10:1) to obtain the title compound (92 mg, 68%) as a colorless oil.

Aufarbeitung

  1. temperaturewhile heating
  2. temperatureunder reflux
  3. extractionfollowed by extraction with ethyl acetate
  4. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  5. filtrationfiltered
  6. concentrationThe filtrate was concentrated under a reduced pressure
  7. customthe residue was purified by silica gel column chromatography (ethyl acetate:methanol=10:1)

Quellen und Nachweise

ORD-Eintrag
ord-7021c0f8a9bd451380fcc00581f585a4
Quelldatensatz
uspto-grants-2010_11
Patentnummer
US07829585B2

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