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Ammonia → 2-(4-Aminophenyl)ethylamine

HRID 1414441
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1414441
[NH2:1][CH2:2][CH2:3][C:4]1[CH:9]=[CH:8][C:7](S([O-])(=O)=O)=[CH:6][CH:5]=1.[K+].[NH2-:15].[K+].N>>[NH2:1][CH2:2][CH2:3][C:4]1[CH:9]=[CH:8][C:7]([NH2:15])=[CH:6][CH:5]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 222AmmoniaHCID 87015Potassium amideHCID 23690036Potassium p-(2-aminoethyl)benzene sulfonate

Produkt 1

HCID 728952-(4-Aminophenyl)ethylamineAusbeute 82,5 %

Versuchsvorschrift

In a 200-ml autoclave were placed 12 grams (0.05 mole) of anhydrous potassium p-(2-aminoethyl)benzene sulfonate, 6.1 grams (0.11 mole) of potassium amide and 55 ml of liquid ammonia in the same manner as in Example 1. The resultant mixture was heated at 135° C for 5 hours. The reaction pressure in the autoclave was 115 atm. during the reaction. After the ammonia was removed, 10 ml of water was added to the reaction mixture for hydrolysis. The product was extracted with ether and the ether was distilled off to produce crude 4-(2-aminoethyl)aniline. The recrystallization thereof from ether gave 5.6 grams of 4-(2-aminoethyl)aniline having a melting point of 62° to 63° C and boiling point of 140° to 142° C/12 mm Hg. Yield was 82.5%.

Aufarbeitung

  1. customThe reaction pressure in the autoclave
  2. customduring the reaction
  3. customAfter the ammonia was removed
  4. addition10 ml of water was added to the reaction mixture for hydrolysis
  5. extractionThe product was extracted with ether
  6. distillationthe ether was distilled off
  7. customto produce crude 4-(2-aminoethyl)aniline
  8. customThe recrystallization

Quellen und Nachweise

ORD-Eintrag
ord-72ce475e7ab74c4b8748713813b0bed0
Quelldatensatz
uspto-grants-1977_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04001313

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