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3-Bromophenol → Pentyl ether

HRID 36149
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 36149
C([Li])(C)(C)C.BrC1C=C(O)C=CC=1.[CH2:14]([O:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])[CH2:15][CH2:16][CH2:17][CH3:18].BrCCCCCOCC1C=CC=CC=1.C([O:46][CH2:47][CH2:48][CH2:49][CH2:50][CH2:51][C:52]1[CH:53]=[C:54]([OH:58])[CH:55]=[CH:56][CH:57]=1)C1C=CC=CC=1>O1CCCC1.C(O)C.[Pd]>[OH:46][CH2:47][CH2:48][CH2:49][CH2:50][CH2:51][C:52]1[CH:53]=[C:54]([OH:58])[CH:55]=[CH:56][CH:57]=1.[CH2:20]([O:19][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18])[CH2:21][CH2:22][CH2:23][CH3:24]
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Komponenten

10

Edukt 5

HCID 115633-BromophenolHCID 12743Pentyl ether2×HCID 14221121Benzyl 5-Bromoamyl EtherHCID 539069383-(Benzyloxypentyl)-phenolHCID 178418306HCID 178418306, Verbindung

Produkt 2

HCID 12743Pentyl ether
HCID 22407972
3-(5-Hydroxypentyl)-phenol

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 23938PalladiumKatalysatorHCID 702EthanolLösungsmittelHCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

At a temperature of -78° C., 19.4 ml of t-butyl lithium (1.7M) is added to 4.0 gm of the above 3-bromo-phenol, n-pentyl ether in 50 mls tetrahydrofuran; and to this is added 3.3 ml of a freshly prepared solution of Li2CuCl3 (0.10M/THF). The mixture is stirred for 10 minutes, and then 4.35 grams of the 1-bromo-5-benzyloxy pentane are added. The reaction is allowed to warm slowly to ambient temperature over 12 hours and is then stirred an additional 24 hours before being quenched with silica gel. After removing the solvent, the mixture is chromatographed over silica gel (1:1 hexane:ether) to yield a crude mixture containing 3-(benzyloxypentyl)-phenol, n-pentyl ether. A solution of 6.0 gm of this crude mixture in ethanol is hydrogenated over 5% Pd on carbon for 5 hours. After filtering through celite and concentrating, pure 3-(5-hydroxypentyl)-phenol, n-pentyl ether is obtained as a clear oil by HPLC chromatography.

Aufarbeitung

  1. stirringis then stirred an additional 24 hours
  2. custombefore being quenched with silica gel
  3. customAfter removing the solvent
  4. customthe mixture is chromatographed over silica gel (1:1 hexane:ether)
  5. customto yield a crude mixture
  6. filtrationAfter filtering through celite
  7. concentrationconcentrating

Quellen und Nachweise

ORD-Eintrag
ord-a33eb14b5e2546bc96b1dbc59ac08fd1
Quelldatensatz
uspto-grants-1995_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05412137

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