Water → 2-Fluoro-4,5-dimethoxybenzene-1-sulfonyl chloride

HRID 856992

Reaktionsgleichung

Reaktionsgleichung von HRID 856992
[F:1][C:2]1[CH:3]=[C:4]([O:10][CH3:11])[C:5]([O:8][CH3:9])=[CH:6][CH:7]=1.[S:12]([Cl:15])(Cl)=[O:13].[OH2:16]>ClCCCl>[F:1][C:2]1[CH:3]=[C:4]([O:10][CH3:11])[C:5]([O:8][CH3:9])=[CH:6][C:7]=1[S:12]([Cl:15])(=[O:13])=[O:16]

Komponenten

5

Reaktionsbedingungen

Temperatur
85 °C

Versuchsvorschrift

To a suspension of sulfur trioxide N,N-dimethylformamide complex (4.108 g, 27 mmol) in 1,2-dichloroethane was added 4-fluoroveratrole (3.49 g, 22 mmol) dropwise. The mixture was slowly heated to 85° C. in an oil bath. After 2.5 h, the solids had dissolved to afford a golden yellow solution. A trace of starting material was still present and heating was continued for a further 4.5 h. The oil bath was removed and thionyl chloride (1.95 ml, 27 mmol) added dropwise. The mixture was heated 4 h at 85° C. and allowed to cool to room temperature. The solution was poured into water and extracted with dichloromethane (3×50 ml), the combined organics washed with water, dried over magnesium sulfate and evaporated. Remaining traces of N,N-dimethylformamide were removed azeotropically with toluene to afford the product as an off-white solid that was used without further purification.

Aufarbeitung

  1. dissolutionthe solids had dissolved
  2. customto afford a golden yellow solution
  3. temperatureheating
  4. waitwas continued for a further 4.5 h
  5. customThe oil bath was removed
  6. temperatureThe mixture was heated 4 h at 85° C.
  7. temperatureto cool to room temperature
  8. extractionextracted with dichloromethane (3×50 ml)
  9. washthe combined organics washed with water
  10. dry with materialdried over magnesium sulfate
  11. customevaporated
  12. customRemaining traces of N,N-dimethylformamide were removed azeotropically with toluene

Quellen und Nachweise

ORD-Eintrag
ord-b855db2249d54a2ba556b403a7519397
Quelldatensatz
uspto-grants-2006_12
Patentnummer
US07144890B2

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