StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

Sodium Carbonate → (2R,5S)-Dimethyl 1-(2-(1,3-dioxoisoindolin-2-yl)ethyl)piperidine-2,5-dicarboxylate

HRID 2395831
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2395831
C(=O)([O-])[O-].[Na+].[Na+].Cl.[CH3:8][O:9][C:10]([C@H:12]1[CH2:17][CH2:16][C@H:15]([C:18]([O:20][CH3:21])=[O:19])[CH2:14][NH:13]1)=[O:11].O([CH2:30][CH2:31][N:32]1[C:36](=[O:37])[C:35]2=[CH:38][CH:39]=[CH:40][CH:41]=[C:34]2[C:33]1=[O:42])S(C(F)(F)F)(=O)=O>O.C(Cl)Cl>[C:33]1(=[O:42])[N:32]([CH2:31][CH2:30][N:13]2[CH2:14][C@@H:15]([C:18]([O:20][CH3:21])=[O:19])[CH2:16][CH2:17][C@@H:12]2[C:10]([O:9][CH3:8])=[O:11])[C:36](=[O:37])[C:35]2=[CH:38][CH:39]=[CH:40][CH:41]=[C:34]12
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 10340Sodium CarbonateHCID 118094652-(1,3-Dioxoisoindolin-2-yl)ethyl trifluoromethanesulfonateHCID 67703709trans-2,5-Piperidine dicarboxylate dimethyl ester hydrochloride

Produkt 1

HCID 21782948(2R,5S)-Dimethyl 1-(2-(1,3-dioxoisoindolin-2-yl)ethyl)piperidine-2,5-dicarboxylateAusbeute 99,1 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962
Water
Lösungsmittel
HCID 6344DichloromethaneLösungsmittel2×

Versuchsvorschrift

To a well-stirred bi-phasic mixture consisting of sodium carbonate (500 g, 4.72 mol) in water (3 liters) and trans-2,5-piperidine dicarboxylate dimethyl ester hydrochloride (280 g, 1.18 mol) in methylene chloride (4.5 liters), a solution of 2-phthalimido-ethyl triflate (417 g, 1.29 mol) in methylene chloride (3 liters) was added in a steady stream over a 3 hour period. The organic layer was separated, and the aqueous layer was extracted with fresh methylene chloride (3 liters). The combined organic extracts were washed with water (3 liters), then with brine (3 liters), dried with anhydrous magnesium sulfate and finally, concentrated in vacuo to a solid. The entire residue was triturated in refluxing ether (3 liters), with vigorous stirring, for 15 minutes. After cooling to ambient temperature, the solution was poured into hexanes (3 liters), and the resulting mixture was stirred for 18 hours. The resulting colorless solid was collected by filtration, and the filter cake was washed with hexanes (1 liter). In vacuo drying afforded 437.3 g (99.1% yield) of the title compound as a colorless solid. TLC Rf (ethyl acetate/methylene chloride =1:1 in volume; iodoplatinate spray): 0.5.

Aufarbeitung

  1. customThe organic layer was separated
  2. extractionthe aqueous layer was extracted with fresh methylene chloride (3 liters)
  3. washThe combined organic extracts were washed with water (3 liters)
  4. dry with materialwith brine (3 liters), dried with anhydrous magnesium sulfate
  5. concentrationfinally, concentrated in vacuo to a solid
  6. customThe entire residue was triturated
  7. temperaturein refluxing ether (3 liters)
  8. additionthe solution was poured into hexanes (3 liters)
  9. filtrationThe resulting colorless solid was collected by filtration
  10. washthe filter cake was washed with hexanes (1 liter)
  11. customIn vacuo drying

Quellen und Nachweise

ORD-Eintrag
ord-206dc1cb824845c28b3980e5141dea43
Quelldatensatz
uspto-grants-1996_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05489688

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion