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Water → 1-[2,4-Bis(trifluoromethyl)benzyl]-2-oxopiperidine-4-carboxylic acid

HRID 1620602
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1620602
[O:1]=[C:2]1[CH2:7][CH:6]([C:8]([OH:10])=[O:9])[CH2:5][CH2:4][NH:3]1.[H-].[Na+].Br[CH2:14][C:15]1[CH:20]=[CH:19][C:18]([C:21]([F:24])([F:23])[F:22])=[CH:17][C:16]=1[C:25]([F:28])([F:27])[F:26].O>O1CCCC1>[F:26][C:25]([F:27])([F:28])[C:16]1[CH:17]=[C:18]([C:21]([F:24])([F:22])[F:23])[CH:19]=[CH:20][C:15]=1[CH2:14][N:3]1[CH2:4][CH2:5][CH:6]([C:8]([OH:10])=[O:9])[CH2:7][C:2]1=[O:1]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 962WaterHCID 24758Sodium hydrideHCID 5188712,4-Bis(trifluoromethyl)benzyl bromideHCID 552860802-Oxopiperidine-4-carboxylic acid

Produkt 1

HCID 866787731-[2,4-Bis(trifluoromethyl)benzyl]-2-oxopiperidine-4-carboxylic acidAusbeute 58,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028
Tetrahydrofuran
Lösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

To a solution of 2-oxopiperidine-4-carboxylic acid (21.3 g) in tetrahydrofuran (300 mL) was added 60% sodium hydride (18 g, containing mineral oil) under cooling to 0° C. The reaction mixture was stirred for 30 min under cooling to 0° C. To the reaction mixture was added dropwise 1-(bromomethyl)-2,4-bis(trifluoromethyl)benzene (46 g) under cooling to 0° C., and the mixture was further stirred at 80° C. for 2 days. Water was added to the reaction mixture under cooling to 0° C., and the mixture was extracted with ethyl acetate. To the aqueous layer was further added 10% hydrochloric acid, and the mixture was extracted with ethyl acetate. The extract was dried over sodium sulfate, and the solvent was evaporated under reduced pressure to give the title compound (32 g).

Aufarbeitung

  1. temperatureunder cooling to 0° C
  2. temperatureunder cooling to 0° C.
  3. stirringthe mixture was further stirred at 80° C. for 2 days
  4. temperatureunder cooling to 0° C.
  5. extractionthe mixture was extracted with ethyl acetate
  6. extractionthe mixture was extracted with ethyl acetate
  7. dry with materialThe extract was dried over sodium sulfate
  8. customthe solvent was evaporated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-6f0cb7cf409f4b6da26145a8fe848f96
Quelldatensatz
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08772277B2

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