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

HRID 2390189
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HRID 2390189 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 4

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

생성물 1

HCID 142895251-Fluoro-4-(propylsulfonyl)benzene수율 87%

시약·촉매·용매 3

HCID 887Methanol용매
HCID 962
Water
용매
HCID 6344Dichloromethane용매

실험 절차

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%).

후처리

  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

출처 및 근거

ORD 기록
ord-0f9931167aee42fe980c388bf99bc466
출처 데이터셋
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08273769B2

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