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Diethyl Ether → 2-(3-Methoxyphenyl)propyl 2-Phenylethyl Ether

HRID 1074503
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1074503
[C:1]1([CH2:7][CH2:8][O:9][CH2:10][C:11]([C:14]2[CH:19]=[CH:18][CH:17]=[C:16]([O:20][CH3:21])[CH:15]=2)(O)[CH3:12])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.P(Cl)(Cl)(Cl)=O.CCOCC.C(=O)([O-])[O-].[Na+].[Na+]>N1C=CC=CC=1>[C:1]1([CH2:7][CH2:8][O:9][CH2:10][CH:11]([C:14]2[CH:19]=[CH:18][CH:17]=[C:16]([O:20][CH3:21])[CH:15]=2)[CH3:12])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 3283Diethyl EtherHCID 10340Sodium CarbonateHCID 24813Phosphorus oxychlorideHCID 20496803HCID 20496803, Verbindung

Produkt 1

HCID 204969232-(3-Methoxyphenyl)propyl 2-Phenylethyl Ether

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1049
Pyridine
Lösungsmittel

Reaktionsbedingungen

Temperatur
20 °C

Versuchsvorschrift

To a 0° C. solution of 2-(3-methoxyphenyl)-2-hydroxypropyl 2-phenylethyl ether (498 mg. 1.74 mmole) in pyridine (2 ml.) is added dropwise phosphorous oxychloride (477 μl., 5.22 mmole). The reaction is allowed to warm to 20° C. over a 1.5 hour period. It is then stirred for 1.5 hours at 20° C. and then added to ether (150 ml.) and 15% sodium carbonate (100 ml.). The organic phase is separated and washed with 15% sodium carbonate (3×50 ml.), dried over magnesium sulfate and evaporated to an oil. The oil is dissolved in absolute ethanol (15 ml.), 10% palladium-on-carbon (100 mg.) added and the mixture stirred under one atmosphere of hydrogen gas. When hydrogen uptake ceases the reaction is filtered through diatomaceous earth and the filtrate evaporated to an oil. The oil is purified via preparative layer chromatography on silica gel plates, eluted twice with 6:1 pentane:ether to yield the title compound.

Aufarbeitung

  1. customThe organic phase is separated
  2. washwashed with 15% sodium carbonate (3×50 ml.)
  3. dry with materialdried over magnesium sulfate
  4. customevaporated to an oil
  5. dissolutionThe oil is dissolved in absolute ethanol (15 ml.)
  6. addition10% palladium-on-carbon (100 mg.) added
  7. stirringthe mixture stirred under one atmosphere of hydrogen gas
  8. filtrationis filtered through diatomaceous earth
  9. customthe filtrate evaporated to an oil
  10. customThe oil is purified via preparative layer chromatography on silica gel plates
  11. washeluted twice with 6:1 pentane

Quellen und Nachweise

ORD-Eintrag
ord-ff6408f8b8454bae98b801f70026f7f2
Quelldatensatz
uspto-grants-1983_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04391827

Notizen zur Reaktion

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