Triisopropyl borate → 4-(2-(Tetrahydro-2H-pyran-2-yloxy)ethoxy)-3-(trifluoromethyl)phenylboronic acid

HRID 2079535ノート

反応式

HRID 2079535 の反応式
[Li]CCCC.Br[C:7]1[CH:22]=[CH:21][C:10]([O:11][CH2:12][CH2:13][O:14][CH:15]2[CH2:20][CH2:19][CH2:18][CH2:17][O:16]2)=[C:9]([C:23]([F:26])([F:25])[F:24])[CH:8]=1.[B:27](OC(C)C)([O:32]C(C)C)[O:28]C(C)C>C1COCC1>[O:16]1[CH2:17][CH2:18][CH2:19][CH2:20][CH:15]1[O:14][CH2:13][CH2:12][O:11][C:10]1[CH:21]=[CH:22][C:7]([B:27]([OH:32])[OH:28])=[CH:8][C:9]=1[C:23]([F:26])([F:25])[F:24]

参加物

5

反応条件

温度
-78 °C

実験手順

BuLi (2.5M, 6 ml) was added dropwise to a solution of 2-(2-(4-bromo-2-(trifluoromethyl)phenoxy)ethoxy)tetrahydro-2H-pyran (5 g) in THF (50 ml) at −78° C. under N2 during 3 minutes. After stirring at −78° C. for another 10 minutes, triisopropyl borate (3.8 ml) was then added dropwise during 2 minutes at −78° C. The mixture was stirred at −78° C. for further 30 minutes, then slowly warmed up to room temperature and stirred at room temperature for 30 minutes. The mixture was then quenched with acetic acid (10% in water, 20 ml), extracted with EtOAc (300 ml), washed with water (200 ml×3), dried over sodium sulphate, solvent removed under reduced pressure, the residue was taken in to toluene and then solvent removed under reduced pressure to take out trace of acetic acid (repeat 3 times, until no acetic acid smell) (4.5 g).

後処理

  1. stirringThe mixture was stirred at −78° C. for further 30 minutes
  2. temperatureslowly warmed up to room temperature
  3. stirringstirred at room temperature for 30 minutes
  4. customThe mixture was then quenched with acetic acid (10% in water, 20 ml)
  5. extractionextracted with EtOAc (300 ml)
  6. washwashed with water (200 ml×3)
  7. dry with materialdried over sodium sulphate, solvent
  8. customremoved under reduced pressure
  9. customsolvent removed under reduced pressure

出典と根拠

ORDレコード
ord-d50061e0373d46a3abe226ad413de469
出典データセット
uspto-grants-2011_04
特許番号
US07932251B2

反応ノート

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