Reaktion #2507831

ord-6d632f961daf4b1d887ac4b6a7a21d85

Reaktionsgleichung

CCCCCC1COc2cc(CBr)c(F)cc2C1
7-bromomethyl-6-fluoro-3-pentylchroman
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
CCCCCC1COc2cc(C[P+](c3ccccc3)(c3ccccc3)c3ccccc3)c(F)cc2C1.[Br-]
(6-Fluoro-3-pentylchroman-7-ylmethyl)triphenylphosphonium bromide

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe batch is subsequently cooled to 0° C.
  2. 2
    Filtrationthe precipitated (6-fluoro-3-pentylchroman-7-ylmethyl)triphenylphosphonium bromide is filtered off with suction
  3. 3
    Sonstigedried in vacuo

Vorschrift

11.0 g (34.9 mmol) of 7-bromomethyl-6-fluoro-3-pentylchroman and 9.20 g (35.1 mmol) of triphenylphosphine are dissolved in 70 ml of acetonitrile, and the mixture is stirred overnight at room temp. The batch is subsequently cooled to 0° C., and the precipitated (6-fluoro-3-pentylchroman-7-ylmethyl)triphenylphosphonium bromide is filtered off with suction and dried in vacuo.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07955664B2uspto-grants-2011_06