Triisopropyl borate → (2,3-Dimethylpyridin-4-YL)boronic acid

HRID 391786

反応式

HRID 391786 の反応式
Br[C:2]1[CH:7]=[CH:6][N:5]=[C:4]([CH3:8])[C:3]=1[CH3:9].[B:10](OC(C)C)([O:15]C(C)C)[O:11]C(C)C.[Li]CCCC>C1COCC1.C1(C)C=CC=CC=1>[CH3:8][C:4]1[C:3]([CH3:9])=[C:2]([B:10]([OH:15])[OH:11])[CH:7]=[CH:6][N:5]=1

参加物

6

反応条件

温度
-20 °C

実験手順

A solution of 4-bromo-2,3-dimethyl-pyridine (1.38 g) and triisopropyl borate (2.05 mL) in 4 mL dry THF and 14 mL dry toluene was stirred on a dry ice-aceton bath to an internal temperature of −65° C. and 3.56 mL n-BuLi in hexanes was added dropwise over 0.5 h. Stirring continued at −65° C. for additional 2 h, then the bath was removed the mixture allowed to warm to −20° C. Reaction was quenched by addition of 10 mL 2M HCl, then allowed to warm to rt and diluted with more THF. 5M NaOH was added until the mixture reached pH 7, layers formed and the organic layer was collected. Several more extractions with THF were done and the combined organic extracts were dried with brine and Na2SO4 and concentrated under reduced pressure. The product crystallized and two crops were collected, for a total of 304 mg of 2,3-dimethylpyridine-4-boronic acid. LCMS (m/z) 153.

後処理

  1. additionwas added dropwise over 0.5 h
  2. customthe bath was removed the mixture
  3. customReaction
  4. customwas quenched by addition of 10 mL 2M HCl
  5. temperatureto warm to rt
  6. additiondiluted with more THF
  7. addition5M NaOH was added until the mixture
  8. customformed
  9. customthe organic layer was collected
  10. extractionSeveral more extractions with THF
  11. dry with materialthe combined organic extracts were dried with brine and Na2SO4
  12. concentrationconcentrated under reduced pressure
  13. customThe product crystallized
  14. customtwo crops were collected, for a total of 304 mg of 2,3-dimethylpyridine-4-boronic acid

出典と根拠

ORDレコード
ord-d0411694b7d8434589e28eb36e26f2d1
出典データセット
uspto-grants-2013_02
特許番号
US08383644B2

関連ノート

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