تفاعل #2348088

ord-c9212347386743b0a31c65a68a16ad30

معادلة التفاعل

Cl
hydrochloric acid
[Li][CH](C)CC
sec-BuLi
Cc1cccc(F)c1F
compound ( 2 )
Cc1cccc(F)c1F
2,3-difluorotoluene
C1CCOC1
THF
COB(OC)OC
trimethyl borate
C1CCOC1
THF
Cc1cc(F)c(F)c(OB(O)O)c1
2,3-difluoro-5-methylphenylboric acid

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwas added
  2. 2
    workup.ADDITIONwas added dropwise
  3. 3
    workup.STIRRINGby stirring at the same temperature for 1 hour
  4. 4
    workup.STIRRINGstirred over night
  5. 5
    درجة الحرارةUnder cooling with an ice bath
  6. 6
    استخلاصThe aqueous layer was extracted with diethyl ether, which
  7. 7
    workup.ADDITIONwas added to the organic layer
  8. 8
    غسيلthe organic layer was washed with a saturated saline
  9. 9
    تجفيفdried over anhydrous magnesium sulfate
  10. 10
    workup.DISTILLATIONThe solvent was distilled off

الإجراء التجريبي

Under a nitrogen atmosphere, 30 g the compound (2) having been dissolved in 240 mL of THF was cooled to −78° C., to which 284 mL of sec-BuLi (1 M/L) was added, followed by stirring at the same temperature for 2 hours. 48.7 g of trimethyl borate having been dissolved in 120 mL of THF was added dropwise thereto at the same temperature, followed by stirring at the same temperature for 1 hour, and the mixture was increased in temperature to room temperature and then stirred over night. Under cooling with an ice bath, 200 mL of 3N hydrochloric acid was added to the mixture. The aqueous layer was extracted with diethyl ether, which was added to the organic layer, and the organic layer was washed with a saturated saline and then dried over anhydrous magnesium sulfate. The solvent was distilled off to obtain 48.8 g of 2,3-difluoro-5-methylphenylboric acid (3), which was used in the next step without purification.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07846513B2uspto-grants-2010_12