Réaction #1519101

ord-2de18b58dc1d42b5b73d66ff38800e42

Équation de réaction

BrC(Br)(Br)Br
Tetrabromomethane
OCC1CC2C=CC1O2
7-oxanorborn-2-en-5-ylmethanol
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
BrCC1CC2C=CC1O2
7-oxanorborn-2-en-5-yl-methyl bromide

Solvants

Conditions de réaction

Température
0°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températureto warm to room temperature
  2. 2
    AutreThe solvent was removed under reduced pressure
  3. 3
    AutreThe crude product was purified by flash chromatography (
  4. 4
    workup.ADDITIONa 98:2 mixture of cyclohexane and ethyl acetate)
  5. 5
    Autre0.3 g (59% of theory) of the pure product were obtained

Mode opératoire

Tetrabromomethane (1.161 g, 3.50 mmol) was added to a solution of 7-oxanorborn-2-en-5-ylmethanol (0.305 g, 2.50 mmol, from Example 2) in CH2Cl2 (12.5 ml). The solution was cooled to 0° C. and admixed with triphenylphosphine (1.836 g, 7 mmol). The reaction mixture was allowed to warm to room temperature and stirred for 12 h. The solvent was removed under reduced pressure and the remaining solid was taken up in cyclohexane. The crude product was purified by flash chromatography (using a 98:2 mixture of cyclohexane and ethyl acetate). 0.3 g (59% of theory) of the pure product were obtained. The product was stored under cool conditions with the exclusion of light.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07612008B2uspto-grants-2009_11