Hydrochloric Acid → 4-(2-Phenyl-1H-benzimidazol-1-yl)phenylboronic Acid (contains varying amounts of Anhydride)

HRID 1172779노트

반응식

HRID 1172779 반응식
BrC1C=CC([C:8]2([N:14]3[C:18]4[CH:19]=[CH:20][CH:21]=[CH:22][C:17]=4[N:16]=[CH:15]3)[CH:13]=[CH:12][CH:11]=[CH:10][CH2:9]2)=CC=1.[CH2:23]([Li])[CH2:24][CH2:25][CH3:26].C[O:29][B:30]([O:33]C)OC.Cl.[CH2:36]1COC[CH2:37]1>>[C:26]1([C:15]2[N:14]([C:8]3[CH:9]=[CH:10][C:11]([B:30]([OH:33])[OH:29])=[CH:12][CH:13]=3)[C:18]3[CH:19]=[CH:20][CH:21]=[CH:22][C:17]=3[N:16]=2)[CH:37]=[CH:36][CH:23]=[CH:24][CH:25]=1

참가 물질

6

반응 조건

온도
-78 °C

실험 절차

In an argon atmosphere, 10 g (29 mmol) of 1-(4-bromophenyl)-phenyl-1H-benzimidazole were dissolved into 100 mL of dehydrated THF, and the temperature of the solution was cooled to −78° C. Then, 20 mL of n-butyllithium (in hexane, 1.6 mol/L) were dropped. After the mixture had been stirred at −78° C. for 1 hour, the temperature of the mixture was increased to 0° C. The temperature of the mixture was cooled to −78° C. again, and 9.7 mL (87 mmol) of trimethoxyborane were dropped. The mixture was stirred at −78° C. for 1 hour, and was then stirred at room temperature for 2 hours. 100 mL of 10-mass % hydrochloric acid were added, and the whole was stirred for 1 hour, followed by filtration. The organic layer of the filtrate was washed with a saturated sodium chloride solution and dried with magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by means of silica gel column chromatography to obtain 4.2 g of 4-(2-phenyl-1H-benzimidazol-1-yl)phenylboronic acid (46% yield).

후처리

  1. temperaturethe temperature of the mixture was increased to 0° C
  2. temperatureThe temperature of the mixture was cooled to −78° C. again
  3. stirringThe mixture was stirred at −78° C. for 1 hour
  4. stirringwas then stirred at room temperature for 2 hours
  5. stirringthe whole was stirred for 1 hour
  6. filtrationfollowed by filtration
  7. washThe organic layer of the filtrate was washed with a saturated sodium chloride solution
  8. dry with materialdried with magnesium sulfate
  9. distillationThe solvent was distilled off under reduced pressure
  10. customthe residue was purified by means of silica gel column chromatography

출처 및 근거

ORD 기록
ord-8553d4b3adb64abfb32f09866707a092
출처 데이터셋
uspto-grants-2010_11
특허 번호
US07833632B2

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