Hydrochloric Acid → 4-ethoxy-2-trifluoromethylphenylboric Acid

HRID 1789631ノート

反応式

HRID 1789631 の反応式
Br[C:2]1[CH:7]=[CH:6][C:5]([O:8][CH2:9][CH3:10])=[CH:4][C:3]=1[C:11]([F:14])([F:13])[F:12].C([Li])CCC.CCCCCC.[B:26]([O:35]C(C)C)([O:31]C(C)C)[O:27]C(C)C.Cl>O1CCCC1>[CH2:9]([O:8][C:5]1[CH:6]=[CH:7][C:2]([O:27][B:26]([OH:35])[OH:31])=[C:3]([C:11]([F:14])([F:13])[F:12])[CH:4]=1)[CH3:10]

参加物

6

反応条件

温度
-78 °C

実験手順

Compound (c) (10.0 g) dissolved in tetrahydrofuran (THF) (40 mL) was cooled to −78° C., a 1.6 M butyllithium/hexane solution (30 mL) was slowly added dropwise and the mixture was stirred at the same temperature for 2 hours. Triisopropyl borate (14.0 g) dissolved in THF (20 mL) was then slowly added dropwise at −78° C., and the mixture was stirred at the same temperature for 1 hour. The temperature was increased to room temperature and the final solution was stirred. After adding 3 M hydrochloric acid (200 mL) dropwise at ice-cooling temperature, the aqueous layer was extracted three times with ether. The organic layers were combined, washed with water and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to obtain 8.28 g of Compound (d).

後処理

  1. additionwas then slowly added dropwise at −78° C.
  2. stirringthe mixture was stirred at the same temperature for 1 hour
  3. temperatureThe temperature was increased to room temperature
  4. temperaturecooling temperature
  5. extractionthe aqueous layer was extracted three times with ether
  6. washwashed with water
  7. dry with materialdried over anhydrous magnesium sulfate
  8. distillationThe solvent was distilled off under reduced pressure

出典と根拠

ORDレコード
ord-5820225fe8974a7692d95ff7a8e72a7a
出典データセット
uspto-grants-2006_07
特許番号
US07070838B2

反応ノート

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