Hydrochloric Acid → 4-[2-(Diethylamino)ethyl]aniline

HRID 641062

Reaktionsgleichung

Reaktionsgleichung von HRID 641062
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([N:11]([CH2:14][CH3:15])[CH2:12][CH3:13])=O)=[CH:4][CH:3]=1.NC1C=CC(CC(N)=O)=CC=1.CSC.B.Cl.[OH-].[Na+]>C1COCC1>[CH2:14]([N:11]([CH2:12][CH3:13])[CH2:9][CH2:8][C:5]1[CH:4]=[CH:3][C:2]([NH2:1])=[CH:7][CH:6]=1)[CH3:15]

Komponenten

7

Edukt 5

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 2380342-(4-Aminophenyl)acetamideHCID 12423031(Dimethyl sulfide)trihydroboronHCID 16775389HCID 16775389, Verbindung

Produkt 1

HCID 225692664-[2-(Diethylamino)ethyl]anilineAusbeute 86 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

To a solution of 2-(4-aminophenyl)-N,N-diethylacetamide, (2-NB-2-A13; 1.5 g, 7.28 mmol) from Step 2 in anhydrous THF (15 mL) kept at 0° C. was added a 2 M solution of borane dimethylsulfide in THF (14.5 mL, 29 mmol) slowly. The reaction was allowed to warm to room temperature and stirred for 18 h. Hydrochloric acid (6N, 10 mL) was carefully added and the reaction was refluxed for 1 hour followed by cooling to room temperature and neutralization with 3N sodium hydroxide solution. Aqueous layer was separated and extracted with ethyl acetate (4×30 mL). Combined organic layer was dried over sodium sulfate, filtered and evaporated to provide 4-(2-(diethylamino)ethyl)aniline as a light-brown oil (1.25 g, 86%).

Aufarbeitung

  1. customkept at 0° C.
  2. temperaturethe reaction was refluxed for 1 hour
  3. temperatureby cooling to room temperature
  4. customAqueous layer was separated
  5. extractionextracted with ethyl acetate (4×30 mL)
  6. dry with materialCombined organic layer was dried over sodium sulfate
  7. filtrationfiltered
  8. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-9f939849868e4113b94cf81b2d00c8cc
Quelldatensatz
uspto-grants-2010_04
Patentnummer
US07692005B2

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