Carbon Dioxide → HCID 12230326, Verbindung

HRID 855284Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 855284
Br[C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:10]=1[NH:9][C:8]([CH3:11])=[CH:7]2.[Li]CCCC.[C:17](=[O:19])=[O:18].O>C1COCC1.CCCCCC>[CH3:11][C:8]1[NH:9][C:10]2[C:6]([CH:7]=1)=[CH:5][CH:4]=[CH:3][C:2]=2[C:17]([OH:19])=[O:18]

Komponenten

7

Reaktionsbedingungen

Temperatur
2.5 °C

Versuchsvorschrift

1000 mg of 7-bromo-2-methyl-indole (4.8 mmol) were dissolved in 15 ml THF and 8.9 ml of a 1.6 molar solution of n-BuLi in hexane were added at −78° C. The reaction mixture was then allowed to warm to 0-5° C. and was stirred at this temperature for 30 min. Then it was cooled again to −78° C., dry ice was added and the mixture was allowed to warm to rt. After 15 min at rt it was poured into water and extracted twice with ether. The aqueous phase was then acidified with 1 N HCl solution and extracted several times with DCM. The combined DCM extracts were then dried with magnesium sulfate, filtered and the solvent was evaporated. The remaining residue was triturated with pentane. Final filtration yielded 157 mg (31%) of 2-methyl-1H-indole-7-carboxylic acid as an off-white solid. MS (ISP) 174.3 (M−H)−.

Aufarbeitung

  1. temperatureThen it was cooled again to −78° C.
  2. temperatureto warm to rt
  3. extractionextracted twice with ether
  4. extractionextracted several times with DCM
  5. dry with materialThe combined DCM extracts were then dried with magnesium sulfate
  6. filtrationfiltered
  7. customthe solvent was evaporated
  8. customThe remaining residue was triturated with pentane
  9. filtrationFinal filtration

Quellen und Nachweise

ORD-Eintrag
ord-9bb3c9e942174166ad9c08e81dbe5e5f
Quelldatensatz
uspto-grants-2007_08
Patentnummer
US07259183B2

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