(4-Nitrophenyl)acetic acid → 1-[(4-Nitrophenyl)acetyl]piperidine

HRID 2219178

Reaktionsgleichung

Reaktionsgleichung von HRID 2219178
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([CH2:10][C:11]([OH:13])=O)=[CH:6][CH:5]=1)([O-:3])=[O:2].[NH:14]1[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]1.C(=O)(O)[O-].[Na+]>O1CCCC1>[N+:1]([C:4]1[CH:5]=[CH:6][C:7]([CH2:10][C:11]([N:14]2[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]2)=[O:13])=[CH:8][CH:9]=1)([O-:3])=[O:2]

Komponenten

5

Versuchsvorschrift

A room temperature solution of 2.53 gms. (4-Nitro-phenyl)-acetic acid in tetrahydrofuran (10 mL) is treated with 2.44 gms. 1′,1′-carbonyl-diimidizole and immediately immersed in an ice bath. The reaction mixture is stirred in the ice bath for 30 minutes then it is allowed to warm to room temperature. Once at room temperature the reaction mixture is treated with 1.21 mL piperidine, and then is stirred overnight at room temperature. The reaction is then made basic with the addition of saturated aqueous sodium bicarbonate, and the resulting mixture is extracted with ethyl acetate. The organics are separated, dried over anhydrous sodium sulfate, filtered, and subsequently evaporated to dryness in vacuo. The crude product residue is then chromatographed by flash silica gel chromatography using 50% ethyl acetate in hexanes as the eluant. Following evaporation of solvent, 2-(4-nitro-phenyl)-1-piperidin-1-yl-ethanone is isolated as a white solid in the amount of 3.18 gms.

Aufarbeitung

  1. customA room temperature solution of 2.53 gms
  2. custom1′,1′-carbonyl-diimidizole and immediately immersed in an ice bath
  3. extractionthe resulting mixture is extracted with ethyl acetate
  4. customThe organics are separated
  5. dry with materialdried over anhydrous sodium sulfate
  6. filtrationfiltered
  7. customsubsequently evaporated to dryness in vacuo
  8. customThe crude product residue is then chromatographed by flash silica gel chromatography
  9. customevaporation of solvent

Quellen und Nachweise

ORD-Eintrag
ord-ff65cd500dd54fb78d476a81135787d4
Quelldatensatz
uspto-grants-2008_08
Patentnummer
US07414054B2

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