3-Bromopyridine → HCID 68899458、化合物

HRID 735359ノート

反応式

HRID 735359 の反応式
[Br:1][C:2]1[CH:3]=[N:4][CH:5]=[CH:6][CH:7]=1.C([N-]C(C)C)(C)C.[Li+].[C:16]1(=[O:20])[CH2:19][CH2:18][CH2:17]1>C1COCC1>[Br:1][C:2]1[CH:3]=[N:4][CH:5]=[CH:6][C:7]=1[C:16]1([OH:20])[CH2:19][CH2:18][CH2:17]1

参加物

5

実験手順

3-Bromopyridine (1 g, 6.3 mmol) was added in a dropwise fashion to a stirred, −78° C. solution of lithium diisopropylamide (1.8 M commercial solution; 3.7 mL, 6.7 mmol) in THF (16 mL). After 10 minutes, cyclobutanone (0.52 mL, 7.0 mmol) was added dropwise and stirring was continued for 1 hour at −78° C., prior to warming to ambient temperature. After stirring for a further 30 minutes, the reaction was quenched by addition of saturated aqueous NH4Cl (10 mL) and the mixture partitioned between EtOAc (100 mL) and water (100 mL). The organic fraction was washed with brine, dried (MgSO4), filtered and concentrated in vacuo. The resulting crude product was purified by flash column chromatography on silica (eluent 50% EOAc/isohexane) to afford 1-(3-bromopyridin-4-yl)cyclobutanol as an off-white solid (412 mg). m/z (ES+) 228/230 [MH+].

後処理

  1. waitwas continued for 1 hour at −78° C.
  2. stirringAfter stirring for a further 30 minutes
  3. customthe reaction was quenched by addition of saturated aqueous NH4Cl (10 mL)
  4. customthe mixture partitioned between EtOAc (100 mL) and water (100 mL)
  5. washThe organic fraction was washed with brine
  6. dry with materialdried (MgSO4)
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. customThe resulting crude product was purified by flash column chromatography on silica (eluent 50% EOAc/isohexane)

出典と根拠

ORDレコード
ord-4b564e529a464f3bb52e30f844814c32
出典データセット
uspto-grants-2009_09
特許番号
US07592456B2

反応ノート

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