Réaction #160659

ord-548a2caffd264bfa9cf739006876a1f8

Équation de réaction

II
iodine
OP(O)O
phosphorous acid
OC(c1ccccc1)c1ccc(Br)cc1
4-Bromobenzhydrol
Brc1ccc(Cc2ccccc2)cc1
4-Bromodiphenylmethane
Rendement 61.0%

Solvants

Conditions de réaction

Température
80°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurecooled
  2. 2
    Extractionthe reaction mixture was extracted with hexane (200 ml) 5 times
  3. 3
    LavageThe combined organic layer was washed with 10 wt. % KOH solution and 200 ml of a saturated ammonium chloride solution
  4. 4
    Lavagefurther washed with a saturated Na2SO3 solution twice
  5. 5
    AutreThe solvent was evaporated
  6. 6
    Autrethe result product was dried under vacuum
  7. 7
    Autreto provide a yield of 61% (276 mmol)

Mode opératoire

4-Bromodiphenylmethane was prepared as shown in Scheme 3. 4-Bromobenzhydrol in a 3-neck flask equipped with a reflux condenser and a thermometer was mixed with 500 ml of acetic acid, 113 g (445 mmol) of iodine and 226 ml, 50 wt. % of phosphorous acid (2.2 mol). The reaction mixture was heated at 80° C. for 24 hours and then cooled. 700 ml of ice-water was added to the reaction mixture and the reaction mixture was extracted with hexane (200 ml) 5 times. The combined organic layer was washed with 10 wt. % KOH solution and 200 ml of a saturated ammonium chloride solution and then further washed with a saturated Na2SO3 solution twice. The solvent was evaporated and the result product was dried under vacuum to provide a yield of 61% (276 mmol). BP: 103° C. (5*10−2 mbar)

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08829155B2uspto-grants-2014_09