Réaction #1960486

ord-f29fcaece21647d98b814a1eb29ba48a

Équation de réaction

[Li][CH2]CCC
n-BuLi
Cl
hydrochloric acid
COB(OC)OC
trimethyl borate
OO
hydrogen peroxide
Fc1ccc2c(c1F)OCCC2
7,8-difluorochroman
Oc1cc2c(c(F)c1F)OCCC2
7,8-difluorochroman-6-ol

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autreat −70° C
  2. 2
    workup.ADDITIONWhen the addition
  3. 3
    ExtractionThe solution is extracted a number of times with MTBE
  4. 4
    Lavagethe combined organic phases are washed successively with water, sat. sodium chloride soln
  5. 5
    AutreThe solution is dried
  6. 6
    Autreevaporated to dryness
  7. 7
    AutreThe crude product is purified by column chromatography (SiO2, n-heptane: MTBE=2:1)

Mode opératoire

81.2 ml (0.13 mol) of n-BuLi (15% soln. in hexane) are added to a soln. of 20.0 g (0.12 mol) of 7,8-difluorochroman in 400 ml of THF at −70° C. After 3 h at this temperature, 14.4 ml (0.13 mol) of trimethyl borate are added dropwise, and the batch is warmed to RT. 30 ml of dilute acetic acid (about 30%) are added, and 30 ml of aqueous hydrogen peroxide solution (35%) are carefully added to the batch. When the addition is complete, the mixture is stirred at RT for 17 h. Water is added, and the batch is acidified using 2 N hydrochloric acid. The solution is extracted a number of times with MTBE, and the combined organic phases are washed successively with water, sat. sodium chloride soln. and ammonium iron(II) sulfate soln. The solution is dried using sodium sulfate and evaporated to dryness. The crude product is purified by column chromatography (SiO2, n-heptane: MTBE=2:1).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08303844B2uspto-grants-2012_11