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Hydrochloric Acid → 2-Methyl-1-phenylpropan-1-amine

HRID 928883
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 928883
COC1C=CC=CC=1[NH:5][CH:6]([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[CH:7]([CH3:9])[CH3:8].S(OOS([O-])(=O)=O)([O-])(=O)=O.[NH4+].[NH4+].Cl>[N+]([O-])([O-])=O.[Ag+].CC#N.O>[CH3:8][CH:7]([CH3:9])[CH:6]([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[NH2:5]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 313Hydrochloric AcidHCID 62648Ammonium PersulfateHCID 107535212-methoxy-N-(2-methyl-1-phenylpropyl)aniline

Produkt 1

HCID 49628752-Methyl-1-phenylpropan-1-amineAusbeute 32,2 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 24470Silver NitrateKatalysator
HCID 18373917
Acetonitrile--water (1/1)
Lösungsmittel

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

To 2-methoxy-N-(2-methyl-1-phenylpropyl)aniline (1.36 g, 5.34 mmol, 1.00 equiv) in 2:1 v/v MeCN/H2O (76 mL) was added AgNO3 (0.271 g, 1.60 mmol, 0.300 equiv) and the reaction mixture was heated to 60° C. Ammonium persulfate (8.58 g, 37.6 mmol, 7.04 equiv) was added in three portions over 15 min and the reaction mixture was heated at 60° C. for 1 h. An aqueous solution of HCl (10 mL, 2 N in H2O) was added. The reaction mixture was filtered through a celite pad, eluting with H2O. The aqueous layer was washed with Et2O (3×30 mL) and the combined organic layers were washed with HCl (2×30 mL, 0.5 N in H2O). The combined aqueous layers were basified with 2.5 M NaOH and the aqueous layer was extracted with Et2O (4×20 mL). The combined organic layers were washed with brine, dried over MgSO4, filtered, and concentrated. The residue was purified by Kugelrohr distillation (50 mTorr, 60° C.) to give 2-methyl-1-phenylpropan-1-amine as a colorless oil (0.257 g, 32% yield).

Aufarbeitung

  1. temperaturethe reaction mixture was heated at 60° C. for 1 h
  2. filtrationThe reaction mixture was filtered through a celite pad
  3. washeluting with H2O
  4. washThe aqueous layer was washed with Et2O (3×30 mL)
  5. washthe combined organic layers were washed with HCl (2×30 mL, 0.5 N in H2O)
  6. extractionthe aqueous layer was extracted with Et2O (4×20 mL)
  7. washThe combined organic layers were washed with brine
  8. dry with materialdried over MgSO4
  9. filtrationfiltered
  10. concentrationconcentrated
  11. distillationThe residue was purified by Kugelrohr distillation (50 mTorr, 60° C.)

Quellen und Nachweise

ORD-Eintrag
ord-2f60aa187bfe4b7f8f4dce50bbf5aa6b
Quelldatensatz
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09290591B2

Notizen zur Reaktion

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