(Diethylamino)sulfur trifluoride → 1-Bromo-4-(1-fluorocyclobutyl)benzene

HRID 19767ノート

反応式

HRID 19767 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2(O)[CH2:11][CH2:10][CH2:9]2)=[CH:4][CH:3]=1.C(N(S(F)(F)[F:19])CC)C>C(Cl)Cl>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2([F:19])[CH2:11][CH2:10][CH2:9]2)=[CH:4][CH:3]=1

参加物

4

反応物 2

HCID 123472(Diethylamino)sulfur trifluorideHCID 120954191-(4-Bromophenyl)cyclobutanol

生成物 1

HCID 685641591-Bromo-4-(1-fluorocyclobutyl)benzene収率 64.1%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
0 °C

実験手順

To a solution of 5.66 g of 1-(4-bromophenyl)-cyclobutanol (24.92 mmol, described in example S2-A) in 70 ml DCM were added 4.23 g of (diethylamino)sulfur trifluoride (95%, 24.92 mmol) at 0° C. The reaction mixture was stirred at 0° C. for 35 min, then sat. NaHCO3— solution was added and the resulting mixture was extracted with DCM. The combined organic extracts were washed with brine, dried (MgSO4), filtered, and concentrated in vacuo to give a residue which was purified by flash column chromatography (100% pentane) to give 1-bromo-4-(1-fluoro-cyclobutyl)-benzene (3.66 g, 64%) as a colorless liquid.

後処理

  1. customat 0° C
  2. extractionthe resulting mixture was extracted with DCM
  3. washThe combined organic extracts were washed with brine
  4. dry with materialdried (MgSO4)
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customto give a residue which
  8. customwas purified by flash column chromatography (100% pentane)

出典と根拠

ORDレコード
ord-8cb30b2a5fa74259aa6b20b955ff6ebf
出典データセット
uspto-grants-2010_06
特許番号
US07745477B2

反応ノート

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