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Potassium Hydroxide → 2-[(4-Fluorophenethyl)oxy]ethylamine

HRID 1422278
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1422278
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][O:10][CH2:11][CH2:12][NH:13]C(=O)OC)=[CH:4][CH:3]=1.[OH-].[K+].O.NN>C(O)CO.O>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][CH2:9][O:10][CH2:11][CH2:12][NH2:13])=[CH:6][CH:7]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 14797Potassium HydroxideHCID 24654Hydrazine hydrate (1:1)HCID 18779044Methyl N-[2-(2-(4-fluorophenyl)ethoxy)ethyl]carbamate

Produkt 1

HCID 187790642-[(4-Fluorophenethyl)oxy]ethylamine

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 174Ethylene GlycolLösungsmittelHCID 962
Water
Lösungsmittel

Versuchsvorschrift

The product of step d) (8.0 g) was dissolved in ethylene glycol and to this was added potassium hydroxide (48 g) and hydrazine hydrate (8.3 ml). The stirred mixture was heated to 140° for 4 hours then allowed to cool to room temperature overnight. The mixture was then diluted with water and extracted with diethyl ether (x3). The combined organic extracts were washed with brine, dried (MgOS4) and filtered. The volatiles were removed in vacuo to give the subtitle compound (5.36 g).

Aufarbeitung

  1. temperatureThe stirred mixture was heated to 140° for 4 hours
  2. extractionextracted with diethyl ether (x3)
  3. washThe combined organic extracts were washed with brine
  4. dry with materialdried (MgOS4)
  5. filtrationfiltered
  6. customThe volatiles were removed in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-b941b40684994b01b2149ef4bbb1fc88
Quelldatensatz
uspto-grants-2000_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06080869

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