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Potassium Carbonate → (R)-2,2-difluoro-hexahydro-5,5-dimethylindolizin-7(1H)-one

HRID 633349
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 633349
[F:1][C:2]1([F:14])[CH2:6][NH:5][C@H:4]([CH2:7][C:8](=[O:13])[CH:9]=[C:10]([CH3:12])[CH3:11])[CH2:3]1.C([O-])([O-])=O.[K+].[K+]>CO>[F:14][C:2]1([F:1])[CH2:6][N:5]2[C@H:4]([CH2:7][C:8](=[O:13])[CH2:9][C:10]2([CH3:11])[CH3:12])[CH2:3]1
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Komponenten

4

Edukt 2

HCID 11430Potassium CarbonateHCID 867044601-((R)-4,4-difluoropyrrolidin-2-yl)-4-methylpent-3-en-2-one

Produkt 1

HCID 86704459(R)-2,2-difluoro-hexahydro-5,5-dimethylindolizin-7(1H)-oneAusbeute 69 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

A MeOH (350 ml) solution of 1-((R)-4,4-difluoropyrrolidin-2-yl)-4-methylpent-3-en-2-one and K2CO3 (2.5 g, 18 mmol) was stirred at 40° C. for 15 hours, the reaction went to completion as monitored by LC-MS. Solvent was removed in vacuo, remaining material was suspended in CH2Cl2, solid was filtered off, filtrate was collected and solvent was removed in vacuo. Product was purified by silica gel chromatography (Hexane/EtOAc, linear gradient from 100:0 to 80:20). Compound (R)-2,2-difluoro-hexahydro-5,5-dimethylindolizin-7(1H)-one was obtained as a light yellow solid: 637.4 mg (69% yield over 3 steps).

Aufarbeitung

  1. customSolvent was removed in vacuo
  2. filtrationsolid was filtered off
  3. customfiltrate was collected
  4. customsolvent was removed in vacuo
  5. customProduct was purified by silica gel chromatography (Hexane/EtOAc, linear gradient from 100:0 to 80:20)

Quellen und Nachweise

ORD-Eintrag
ord-c7a2665a97194efba2650730c0d0d64b
Quelldatensatz
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09321763B2

Notizen zur Reaktion

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