Phenol → HCID 13055710, Verbindung

HRID 2198846Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2198846
[CH:1]([N:4]1[CH2:7][CH:6]([O:8][CH2:9][O:10][CH3:11])[CH2:5]1)([CH3:3])[CH3:2].[C:12]1([OH:18])[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.[OH-].[Na+]>CCOCC>[O:18]([CH2:5][CH:6]([O:8][CH2:9][O:10][CH3:11])[CH2:7][NH:4][CH:1]([CH3:2])[CH3:3])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1

Komponenten

5

Edukt 3

HCID 996PhenolHCID 14798Sodium HydroxideHCID 205173143-(Methoxymethoxy)-1-(propan-2-yl)azetidine

Produkt 1

HCID 13055710HCID 13055710, VerbindungAusbeute 67 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3283Diethyl EtherLösungsmittel

Reaktionsbedingungen

Temperatur
180 °C

Versuchsvorschrift

To a mixture of 1.6 parts of 1-iso-propyl-3-methoxymethoxyazetidine and 9.4 parts of phenol 0.5 part of sodium hydroxide was addded, and the mixture was heated at 180° C. for 6 hours. The reaction mixture was cooled and 100 parts of ether were added thereto. Excessive phenol was removed by extraction with 2 N-sodium hydroxide aqueous solution, and the remaining ether layer was washed in water and dried over anhydrous sodium sulfate. After distillation of ether, the residue was subjected to distillation to yield 1.6 parts of 1-phenoxy-2-methoxymethoxy-3-(iso-propylamino)-propane boiling at 146°-149° C. under 2 mm Hg. The yield was 67%.

Aufarbeitung

  1. temperatureThe reaction mixture was cooled
  2. customExcessive phenol was removed by extraction with 2 N-sodium hydroxide aqueous solution
  3. washthe remaining ether layer was washed in water
  4. dry with materialdried over anhydrous sodium sulfate
  5. distillationAfter distillation of ether
  6. distillationthe residue was subjected to distillation

Quellen und Nachweise

ORD-Eintrag
ord-2c1f4e08a2ae4f29958bfbdb7772391f
Quelldatensatz
uspto-grants-1982_11
Patentnummer
US04360464

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