Potassium Carbonate → 1-(3-Bromopropylsulfanyl)-3,5-difluorobenzene

HRID 1173754ノート

反応式

HRID 1173754 の反応式
[F:1][C:2]1[CH:3]=[C:4]([SH:9])[CH:5]=[C:6]([F:8])[CH:7]=1.[Br:10][CH2:11][CH2:12][CH2:13]O.C(=O)([O-])[O-].[K+].[K+].[Br-].[Br-].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>C(#N)C>[Br:10][CH2:11][CH2:12][CH2:13][S:9][C:4]1[CH:3]=[C:2]([F:1])[CH:7]=[C:6]([F:8])[CH:5]=1

参加物

6

実験手順

To a round-bottom flask was added 3,5-difluorobenzenethiol (4.9 g, 33.8 mmol) in ACN (50 mL). 3-Bromo-1-propanol (4.7 g, 34.0 mmol) and potassium carbonate (6.4 g, 46 mmol) were added, and the mixture was stirred at room temperature for 3 hours. The mixture was then filtered through a pad of Celite® and the solvent was removed under reduced pressure. The crude material was then dissolved in anhydrous DCM (100 mL). Triphenylphosphine dibromide (25 g, 59 mmol) was added to the mixture, which was then stirred for 2 hours. The solvent was removed under reduced pressure. The residue was suspended in EtOAc (200 mL), stirred for 1 hour, and filtered to remove solids. The filtrate was concentrated under reduced pressure, then diluted in 50% EtOAc/hexanes (200 mL), and filtered through a pad of Celite® and silica gel. The solution was then concentrated under reduced pressure to afford the title compound (5.8 g).

後処理

  1. filtrationThe mixture was then filtered through a pad of Celite®
  2. customthe solvent was removed under reduced pressure
  3. dissolutionThe crude material was then dissolved in anhydrous DCM (100 mL)
  4. stirringwas then stirred for 2 hours
  5. customThe solvent was removed under reduced pressure
  6. stirringstirred for 1 hour
  7. filtrationfiltered
  8. customto remove solids
  9. concentrationThe filtrate was concentrated under reduced pressure
  10. additiondiluted in 50% EtOAc/hexanes (200 mL)
  11. filtrationfiltered through a pad of Celite® and silica gel
  12. concentrationThe solution was then concentrated under reduced pressure

出典と根拠

ORDレコード
ord-b8ae22a32d654bab81efd847a3f78876
出典データセット
uspto-grants-2010_11
特許番号
US07834185B2

反応ノート

読み込み中…