Triisopropyl borate → 3,5-Dimethylisoxazole-4-boronic acid

HRID 922262노트

반응식

HRID 922262 반응식
Br[C:2]1[C:3]([CH3:8])=[N:4][O:5][C:6]=1[CH3:7].C([Li])CCC.[B:14](OC(C)C)([O:19]C(C)C)[O:15]C(C)C>C1COCC1>[CH3:8][C:3]1[C:2]([B:14]([OH:19])[OH:15])=[C:6]([CH3:7])[O:5][N:4]=1

참가 물질

5

반응 조건

온도
-78 °C

실험 절차

To a 500 mL three RB flask fitted with magnetic stirrer was charged 4-bromo-3,5-dimethyl-1,2-oxazole (4.0 g, 22.7 mmol) in THF (40 mL), cooled −78° C. To the stirred solvent was added n-butyl lithium (28.4 mL, 1.6M solution, 45.0 mmol) drop wise and stirred at −65° C. about 30 minutes. The RM was brought to −78° C., was added tri-isopropyl borate (12.81 g, 68.0 mmol), once the temperature to reached room temperature and stirred about 16 h. Then removed the solvent under reduced pressure and quenched with saturated NH4Cl solution and extracted with ethyl acetate. The organic layer was washed with water, dried over anhydrous Na2SO4 and removed the solvent under reduced pressure. The obtained crude material was purified by silica gel column chromatography to obtain white solid. (0.4 g, yield: 12.5%).

후처리

  1. customwas brought to −78° C.
  2. customto reached room temperature
  3. stirringstirred about 16 h
  4. customThen removed the solvent under reduced pressure
  5. customquenched with saturated NH4Cl solution
  6. extractionextracted with ethyl acetate
  7. washThe organic layer was washed with water
  8. dry with materialdried over anhydrous Na2SO4
  9. customremoved the solvent under reduced pressure
  10. customThe obtained crude material
  11. customwas purified by silica gel column chromatography
  12. customto obtain white solid

출처 및 근거

ORD 기록
ord-efdcd2fa9b954c05b0076458ad826a1c
출처 데이터셋
uspto-grants-2016_03
특허 번호
US09278915B2

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