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N,N-Dimethylaniline → HCID 19077574, Verbindung

HRID 964607
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 964607
[Cl:1]C(Cl)(Cl)C(Cl)=O.[CH3:8][O:9][C:10]1[CH:17]=[CH:16][C:13]([CH2:14]O)=[CH:12][CH:11]=1.CN(C)C1C=CC=CC=1.[NH:27]1[CH2:32][CH2:31][CH2:30][CH:29]([C:33]([O:35][CH2:36][CH3:37])=[O:34])[CH2:28]1.C(=O)([O-])[O-].[K+].[K+]>C1(C)C=CC=CC=1.ClCCl.CCCCCC.C(OCC)(=O)C>[ClH:1].[CH3:8][O:9][C:10]1[CH:17]=[CH:16][C:13]([CH2:14][N:27]2[CH2:32][CH2:31][CH2:30][CH:29]([C:33]([O:35][CH2:36][CH3:37])=[O:34])[CH2:28]2)=[CH:12][CH:11]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

10

Edukt 5

HCID 949N,N-DimethylanilineHCID 6420Trichloroacetyl chlorideHCID 77384-Methoxybenzyl alcoholHCID 11430Potassium CarbonateHCID 98969Ethyl nipecotate

Produkt 1

HCID 19077574HCID 19077574, VerbindungAusbeute 21,6 %

Reagenzien, Katalysatoren, Lösungsmittel

4
HCID 1140TolueneLösungsmittel2×HCID 6344DichloromethaneLösungsmittelHCID 8058HexaneLösungsmittelHCID 8857Ethyl AcetateLösungsmittel

Versuchsvorschrift

A solution of trichloroacetyl chloride (11.1 ml, 99 mmol) in toluene (30 ml) was added dropwise over 45 minutes to a stirred, ice-cooled solution of 4-methoxybenzyl alcohol (12.4 ml, 99 mmol) and N,N-dimethylaniline (12.6 ml, 99 mmol) in toluene (100 ml). The cooling bath was removed and stirring continued at room temperature for 1.5 hours, then the reaction mixture was filtered to remove the N,N-dimethylaniline hydrochloride which was washed with toluene (30 ml). A stirred mixture of the combined filtrate and washings, ethyl 3-piperidinecarboxylate (14.0 ml, 90 mmol) and anhydrous potassium carbonate (13.7 g, 99 mmol), under nitrogen, was heated under reflux for 110 hours, allowed to cool and filtered. Evaporation of the filtrate under reduced pressure gave a brown oil which was dissolved in dichloromethane (100 ml) and the resulting solution washed successively with 2M aqueous sodium carbonate solution (100 ml) and ca. 5M hydrochloric acid (200 ml), dried (Na2SO4) and evaporated under reduced pressure to provide a viscous oil. This oil was stirred at room temperature with a 1:1 mixture of ethyl acetate:hexane (100 ml) to produce a solid which was purified by successive trituration with the same solvent mixture (4×50 ml) to afford the title compound (6.11 g). Rf 0.85 (SS 1). Found: C,59.41; H,7.50; N,4.15. C16H23NO3 ; HCl; 0.50 H2O requires C,59.52; H,7.80; N,4.34%

Aufarbeitung

  1. customThe cooling bath was removed
  2. filtrationthe reaction mixture was filtered
  3. customto remove the N,N-dimethylaniline hydrochloride which
  4. washwas washed with toluene (30 ml)
  5. temperatureunder nitrogen, was heated
  6. temperatureunder reflux for 110 hours
  7. temperatureto cool
  8. filtrationfiltered
  9. customEvaporation of the filtrate under reduced pressure
  10. customgave a brown oil which
  11. washthe resulting solution washed successively with 2M aqueous sodium carbonate solution (100 ml) and ca. 5M hydrochloric acid (200 ml)
  12. dry with materialdried (Na2SO4)
  13. customevaporated under reduced pressure
  14. customto provide a viscous oil
  15. customwas purified by successive trituration with the same solvent mixture (4×50 ml)

Quellen und Nachweise

ORD-Eintrag
ord-3a3f5f2515594bd396ff59c394984ec1
Quelldatensatz
uspto-grants-1998_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05770611

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