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N-(3-Chlorophenyl)acetamide → N-[3-(Dibutylamino)phenyl]acetamide

HRID 1354980
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1354980
[CH3:1][C:2]([NH:4][C:5]1[CH:10]=[CH:9][CH:8]=[C:7](Cl)[CH:6]=1)=[O:3].C[C:13]([CH3:16])([O-])[CH3:14].[Na+]>C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd].C1(P(C2CCCCC2)C2C=CC=CC=2C2C(C(C)C)=CC(C(C)C)=CC=2C(C)C)CCCCC1>[CH2:5]([N:4]([CH2:2][CH2:14][CH2:13][CH3:16])[C:7]1[CH:6]=[C:5]([NH:4][C:2](=[O:3])[CH3:1])[CH:10]=[CH:9][CH:8]=1)[CH2:6][CH2:7][CH3:8]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 11493N-(3-Chlorophenyl)acetamideHCID 23676156Sodium t-butoxide

Produkt 1

HCID 13879300N-[3-(Dibutylamino)phenyl]acetamideAusbeute 161,6 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 9811564Bis(dibenzylideneacetone)palladiumKatalysatorHCID 11155794
2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl
Katalysator

Versuchsvorschrift

An oven-dried resealable schlenk tube containing a stir bar was charged with Pd2(dba)3 (4.6 mg, 0.005 mmol), 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl (11.9 mg, 0.025 mmol), 3-chloroacetanilide (85 mg, 0.5 mmol) and sodium tbutoxide (120 mg, 1.25 mmol). The tube was capped with a rubber septum, evacuated and backfilled with argon. Dinbutylamine (126 μL, 0.75 mmol) and tbutanol (1 mL) were added through the septum via syringe. The septum was replaced with a Teflon screw cap. The schlenk tube was sealed and put into a pre-heated oil bath at 90° C. The reaction mixture was stirred for 18 h, allowed to cool down to room temperature and quenched with water. Extraction with ethyl acetate three times followed by chromatography on silica gel column with 4:1 hexane:ethyl acetate gave 106 mg (81%) of the title compound as a pale yellow oil.

Aufarbeitung

  1. additionAn oven-dried resealable schlenk tube containing a stir bar
  2. customThe tube was capped with a rubber septum
  3. customevacuated
  4. additionDinbutylamine (126 μL, 0.75 mmol) and tbutanol (1 mL) were added through the septum via syringe
  5. customscrew cap
  6. customThe schlenk tube was sealed
  7. customput into a pre-heated oil bath at 90° C
  8. customquenched with water
  9. extractionExtraction with ethyl acetate three times

Quellen und Nachweise

ORD-Eintrag
ord-5e83fbd8bb524de3bab2ce767bba3562
Quelldatensatz
uspto-grants-2007_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07223879B2

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