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Sodium Hydroxide → 1-Fluoro-4-(propylsulfonyl)benzene

HRID 2390189
ノート
印刷プレビュー

反応式

HRID 2390189 の反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([SH:8])=[CH:4][CH:3]=1.[OH-:9].[Na+].I[CH2:12][CH2:13][CH3:14].ClC1C=CC=C(C(OO)=[O:23])C=1>CO.O.C(Cl)Cl>[F:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([CH2:12][CH2:13][CH3:14])(=[O:23])=[O:9])=[CH:4][CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 14798Sodium HydroxideHCID 336431-IodopropaneHCID 677894-FluorothiophenolHCID 70297m-Chloroperbenzoic acid

生成物 1

HCID 142895251-Fluoro-4-(propylsulfonyl)benzene収率 87%

試薬・触媒・溶媒 3

HCID 887Methanol溶媒
HCID 962
Water
溶媒
HCID 6344Dichloromethane溶媒

実験手順

A cooled (0° C.) solution of 4-fluorothiophenol (Merck Kgaa; 2.00 g; 15.6 mmol) in MeOH (40 ml) was treated with a 5 N solution of NaOH in water (3.28 ml) and 1-iodopropane (1.67 ml; 17.2 mmol). The reaction mixture was stirred at RT for 1 hour, the mixture was concentrated under reduced pressure, the residue taken up in EtOAc and washed with brine, dried on MgSO4, filtered and concentrated under reduced pressure. The intermediate thus obtained was dissolved in DCM (50 ml) and treated with 3-chloroperbenzoic acid (8.46 g; 34.33 mmol) and stirred at RT for 3 hours. The solvent was removed under reduced pressure, the residue taken up in EtOAc and washed with brine, dried on MgSO4, filtered and concentrated under reduced pressure to afford the title compound (2.75 g, 87%).

後処理

  1. concentrationthe mixture was concentrated under reduced pressure
  2. washwashed with brine
  3. customdried on MgSO4
  4. filtrationfiltered
  5. concentrationconcentrated under reduced pressure
  6. customThe intermediate thus obtained
  7. stirringstirred at RT for 3 hours
  8. customThe solvent was removed under reduced pressure
  9. washwashed with brine
  10. customdried on MgSO4
  11. filtrationfiltered
  12. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-0f9931167aee42fe980c388bf99bc466
出典データセット
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08273769B2

反応ノート

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