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Hydrochloric Acid → 2-Methoxy-3-(trifluoromethyl)phenylboronic acid

HRID 2198056
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HRID 2198056 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[C:9]([F:12])([F:11])[F:10].[Li]CCCC.CC([O:21][B:22](OC(C)C)[O:23]C(C)C)C.Cl.COC1C(C(F)(F)F)=C(B(O)O)C=CC=1>C1COCC1>[CH3:1][O:2][C:3]1[C:4]([C:9]([F:10])([F:11])[F:12])=[CH:5][CH:6]=[CH:7][C:8]=1[B:22]([OH:23])[OH:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 313Hydrochloric AcidHCID 21531Triisopropyl borateHCID 27752511-Methoxy-2-(trifluoromethyl)benzeneHCID 670223113-Methoxy-2-(trifluoromethyl)phenylboronic acidHCID 178418339Butyllithium

생성물 1

HCID 453584302-Methoxy-3-(trifluoromethyl)phenylboronic acid수율 83%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 1-methoxy-2-(trifluoromethyl)benzene (6.30 g, 35.8 mmol) in THF (150 mL) was added n-BuLi (21.0 ml, 2.50 M hexane solution, 53.7 mmol), and the mixture was stirred at room temperature for 1 hr. The solution was cooled to −78° C., tris(1-methylethyl)borate (8.08 g, 43.0 mmol) was added, and the mixture was stirred at −78° C. for 0.5 hr. The reaction solution was allowed to cool to room temperature and stirred for 16 hr. The mixture was acidified with 1M hydrochloric acid and extracted with ethyl acetate (300 mL). The extract was dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to give a mixture (6.52 g, yield 83%) of [2-methoxy-3-(trifluoromethyl)phenyl]boronic acid and [3-methoxy-2-(trifluoromethyl)phenyl]boronic acid.

후처리

  1. temperatureThe solution was cooled to −78° C.
  2. stirringthe mixture was stirred at −78° C. for 0.5 hr
  3. temperatureto cool to room temperature
  4. stirringstirred for 16 hr
  5. extractionextracted with ethyl acetate (300 mL)
  6. dry with materialThe extract was dried over anhydrous sodium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-694e63a1b94743f18cb1119bbb1180c5
출처 데이터셋
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08338622B2

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