Reaktion #2314278

ord-9bd666e9f4f14fe9be6a07496a31982b

Reaktionsgleichung

BrC(Br)(Br)Br
tetrabromomethane
OCCCc1ccc(O)cc1
3-(4-hydroxyphenyl)-1-propanol
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
Oc1ccc(CCCBr)cc1
3-(4-hydroxyphenyl)-1-bromopropane
Ausbeute 62.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionextracted with dichloromethane
  2. 2
    Waschenthe organic layer was washed with water
  3. 3
    Trocknendried over anhydrous magnesium sulfate
  4. 4
    SonstigeThe solvent was removed in vacuo
  5. 5
    Sonstigethe crude reaction mixture
  6. 6
    Filtrationwas filtered through silica gel
  7. 7
    Wascheneluting with 10% ethyl acetate in hexane

Vorschrift

A solution of tetrabromomethane (1.125 eq.) in dichloromethane (0.5 ml/mole) was added dropwise to the solution of the commercially available 3-(4-hydroxyphenyl)-1-propanol 1B (1 eq.) and triphenylphosphine (1.125 eq.) in dichloromethane at 0° C. The reaction mixture was stirred at room temperature for 2 days, extracted with dichloromethane, and the organic layer was washed with water and dried over anhydrous magnesium sulfate. The solvent was removed in vacuo. the crude reaction mixture was filtered through silica gel, eluting with 10% ethyl acetate in hexane, to give 3-(4-hydroxyphenyl)-1-bromopropane 2 as a brown oil in 62% yield.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06413448B1uspto-grants-2002_07