Acrylic Acid → 3-(6-Fluoroindolyl)propionic acid

HRID 51015

Reaktionsgleichung

Reaktionsgleichung von HRID 51015
[F:1][C:2]1[CH:10]=[C:9]2[C:5]([CH:6]=[CH:7][NH:8]2)=[CH:4][CH:3]=1.[C:11]([OH:15])(=[O:14])[CH:12]=[CH2:13].C(OC(=O)C)(=O)C>C(O)(=O)C>[F:1][C:2]1[CH:10]=[C:9]2[C:5]([CH:6]=[C:7]([CH2:13][CH2:12][C:11]([OH:15])=[O:14])[NH:8]2)=[CH:4][CH:3]=1

Komponenten

5

Edukt 3

HCID 6581Acrylic AcidHCID 7918Acetic AnhydrideHCID 3512786-Fluoroindole

Produkt 1

HCID 227354403-(6-Fluoroindolyl)propionic acidAusbeute 52,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 176Acetic AcidLösungsmittel

Reaktionsbedingungen

Temperatur
20 °C

Versuchsvorschrift

The solution of 6-fluoroindol (300 mg, 2.22 mmol), acrylic acid (352 mg, 4.88 mmol) and acetic anhydride (453 mg, 4.44 mmol) in acetic acid (1.1 mL) was heated at 90° C. for 15 h. The reaction mixture was cooled to 20° C. then concentrated in vacuo. The residue was dissolved in 3N NaOH. The solution was filtered to remove insoluble material and the filtrate was acidified with conc. HCl and extracted with CHCl3. The organic solution was dried over MgSO4, filtered and concentrated in vacuo to give 3-(6-fluoroindolyl)propionic acid (240 mg, 52%) as a yellow solid.

Aufarbeitung

  1. concentrationthen concentrated in vacuo
  2. dissolutionThe residue was dissolved in 3N NaOH
  3. filtrationThe solution was filtered
  4. customto remove insoluble material
  5. extractionextracted with CHCl3
  6. dry with materialThe organic solution was dried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-61a35a6cba8d448c9e877ac59f2c482e
Quelldatensatz
uspto-grants-2004_03
Patentnummer
US06713471B1

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