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Lithium Hydroxide → 4,6-dimethyl-1H-indole-2-carboxylic Acid

HRID 507327
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 507327
C([O:3][C:4]([C:6]1[NH:7][C:8]2[C:13]([CH:14]=1)=[C:12]([CH3:15])[CH:11]=[C:10]([CH3:16])[CH:9]=2)=[O:5])C.[OH-].[Li+]>C(O)C>[CH3:15][C:12]1[CH:11]=[C:10]([CH3:16])[CH:9]=[C:8]2[C:13]=1[CH:14]=[C:6]([C:4]([OH:5])=[O:3])[NH:7]2
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Komponenten

4

Edukt 2

HCID 3939Lithium HydroxideHCID 4714990ethyl 4,6-dimethyl-1H-indole-2-carboxylate

Produkt 1

HCID 34459014,6-dimethyl-1H-indole-2-carboxylic AcidAusbeute 95,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

A mixture of 4,6-dimethyl-1H-indole-2-carboxylic acid ethyl ester (22 g, 0.1 mol) and lithium hydroxide (4.8 g, 0.2 mol) in 400 ml of ethanol was heated at reflux overnight. The solvent was removed under reduced pressure and the residue was dissolved in water and neutralized with 10% HCl to pH<3. The resulting precipitates were filtered and washed with water and dried in vacuo at 40° C. to give white solids (18 g, 95%). 1H NMR (DMSO-d6, 400 MHz): δ 12.73 (brs, 1H, exchangeable with D2O, NH), 11.55 (brs, 1H, exchangeable with D2O, NH), 7.06 (s, 1H), 7.03 (s, 1H), 6.69 (s, 1H), 2.44 (s, 3H), 2.35 (s, 3H).

Aufarbeitung

  1. temperaturewas heated
  2. temperatureat reflux overnight
  3. customThe solvent was removed under reduced pressure
  4. dissolutionthe residue was dissolved in water and neutralized with 10% HCl to pH<3
  5. customThe resulting precipitates
  6. filtrationwere filtered
  7. washwashed with water
  8. customdried in vacuo at 40° C.

Quellen und Nachweise

ORD-Eintrag
ord-0c44b5b082f8490b88e20f286dde305c
Quelldatensatz
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07786146B2

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