Triphenylphosphine → (8-Tetrahydropyranyloxyoctyl)triphenylphosphonium bromide

HRID 1709074

Reaktionsgleichung

Reaktionsgleichung von HRID 1709074
[Br:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][O:10][CH:11]1[CH2:16][CH2:15][CH2:14][CH2:13][O:12]1.[C:17]1([P:23]([C:30]2[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=2)[C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>C(#N)C>[Br-:1].[O:12]1[CH2:13][CH2:14][CH2:15][CH2:16][CH:11]1[O:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][P+:23]([C:24]1[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=1)([C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1)[C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1

Komponenten

4

Edukt 2

HCID 11776TriphenylphosphineHCID 1709162H-Pyran, 2-[(8-bromooctyl)oxy]tetrahydro-

Produkt 1

HCID 18997637(8-Tetrahydropyranyloxyoctyl)triphenylphosphonium bromide

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6342AcetonitrileLösungsmittel

Versuchsvorschrift

A solution of 1-bromo-8-tetrahydropyranyloxyoctane (9.8 g) and triphenyl phosphine (8.8 g) in acetonitrile (50 ml) was heated under reflux for 8 hours. The solution was evaporated and the residue washed with ether to give the title compound as a hygroscopic white solid which was dried by addition of benzene and re-evaporation.

Aufarbeitung

  1. temperatureunder reflux for 8 hours
  2. customThe solution was evaporated
  3. washthe residue washed with ether

Quellen und Nachweise

ORD-Eintrag
ord-c26ccbbd183d4a589a47a16aad0de11c
Quelldatensatz
uspto-grants-1990_08
Patentnummer
USRE033300

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