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Tetrahydrofuran → 4-(4-Fluorophenyl)-3-formylpiperidine-6-one

HRID 2296770
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2296770
CC(C[AlH]CC(C)C)C.C(C[CH2:14][CH:15]1[CH:20]([C:21]2[CH:26]=[CH:25][C:24]([F:27])=[CH:23][CH:22]=2)[CH2:19][C:18](=[O:28])[NH:17][CH2:16]1)(O)=O.[O:29]1CCCC1>>[F:27][C:24]1[CH:25]=[CH:26][C:21]([CH:20]2[CH2:19][C:18](=[O:28])[NH:17][CH2:16][CH:15]2[CH:14]=[O:29])=[CH:22][CH:23]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 8028TetrahydrofuranHCID 14487Diisobutylaluminum hydrideHCID 227338414-(4-Fluorophenyl)-3-carboxyethylpiperidin-6-one

Produkt 1

HCID 227338454-(4-Fluorophenyl)-3-formylpiperidine-6-one

Reaktionsbedingungen

Temperatur
-70 °C

Versuchsvorschrift

DIBAL-H (4.03 ml, 6 mmol) was added gradually at a rate of 5.6 ml/hour, by means of a syringe pump, to a solution of 3-carboxyethyl-4-(4-fluorophenyl)-piperidine-6-one (0.53 g, 2 mmol) in 4 ml tetrahydrofuran at −70° C. under an argon atmosphere. The reaction mixture was stirred for 1 hour at −70° C. then quenched with a solution of methanol (0.24 ml) in toluene (2 ml) at −70° C., followed by 0.12 ml water at 0° C. After 30 minutes stirring at ambient temperature, the gel which formed was destroyed by the addition of 1.5 ml brine and the reaction mixture was extracted with diethyl ether (50 ml). The organic phase was separated, dried with anhydrous sodium sulphate, filtered and evaporated to yield the title compound (0.2 g) as a yellow oil. The aqueous layer was basified with 10% aqueous sodium hydroxide and extracted with dichloromethane (20 ml). A further 0.08 g product was isolated from the dichloromethane extract.

Aufarbeitung

  1. customat −70° C.
  2. customthen quenched with a solution of methanol (0.24 ml) in toluene (2 ml) at −70° C.
  3. customfollowed by 0.12 ml water at 0° C
  4. stirringAfter 30 minutes stirring at ambient temperature
  5. customthe gel which formed
  6. customwas destroyed by the addition of 1.5 ml brine
  7. extractionthe reaction mixture was extracted with diethyl ether (50 ml)
  8. customThe organic phase was separated
  9. dry with materialdried with anhydrous sodium sulphate
  10. filtrationfiltered
  11. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-686be3697c9340988bd955052b8b0dc7
Quelldatensatz
uspto-grants-2002_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06489347B1

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