Hexamethylphosphoramide → HCID 86681263, Verbindung

HRID 336589

Reaktionsgleichung

Reaktionsgleichung von HRID 336589
[Br:1][C:2]1[C:3]([CH3:9])=[C:4]([OH:8])[CH:5]=[CH:6][CH:7]=1.Br[C:11]12[CH2:20][CH:15]3[CH2:16][CH:17]([CH2:19][CH:13]([CH2:14]3)[CH2:12]1)[CH2:18]2.CN(C)P(N(C)C)(N(C)C)=O>C(OCC)C>[Br:1][C:2]1[C:3]([CH3:9])=[C:4]([CH:5]=[CH:6][CH:7]=1)[O:8][C:11]12[CH2:20][CH:15]3[CH2:16][CH:17]([CH2:19][CH:13]([CH2:14]3)[CH2:12]1)[CH2:18]2

Komponenten

5

Edukt 3

HCID 12679HexamethylphosphoramideHCID 791061-BromoadamantaneHCID 111714303-Bromo-2-methylphenol

Produkt 1

HCID 86681263HCID 86681263, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3283Diethyl EtherLösungsmittel

Reaktionsbedingungen

Temperatur
250 °C

Versuchsvorschrift

3-Bromo-2-methylphenol (1000 mg) and 1-bromoadamantane (2013 mg) were added to hexamethylphosphoramide (8 mL) and the mixture was heated in a microwave reactor (Biotage) at 250° C. for 35 minutes. The solution was taken up in diethyl ether, washed with water two times, washed with brine, dried on anhydrous sodium sulfate, filtered, and concentrated. The crude material was purified by flash column chromatography on silica gel using 2% ethyl acetate (hexanes) increasing to 5% ethyl acetate (hexanes) to yield the title compound.

Aufarbeitung

  1. washwashed with water two times
  2. washwashed with brine
  3. dry with materialdried on anhydrous sodium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe crude material was purified by flash column chromatography on silica gel using 2% ethyl acetate (hexanes)
  7. temperatureincreasing to 5% ethyl acetate (hexanes)

Quellen und Nachweise

ORD-Eintrag
ord-32df780e4a2c43c38b62dc29c3a6c1f6
Quelldatensatz
uspto-grants-2014_11
Patentnummer
US08889675B2

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