Dimethyl Disulfide → (2-Chloro-6-fluorophenyl)(methyl)sulfane

HRID 341743

Reaktionsgleichung

Reaktionsgleichung von HRID 341743
[F:1][C:2]1[CH:3]=[C:4]([Cl:8])[CH:5]=[CH:6][CH:7]=1.[CH3:9][S:10]SC>CCCCCC.O1CCCC1>[Cl:8][C:4]1[CH:5]=[CH:6][CH:7]=[C:2]([F:1])[C:3]=1[S:10][CH3:9]

Komponenten

5

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

n-Butylithium (2.5M in hexane, 129 ml) was added to a solution of 3-fluorochlorobenzene (35 g) in dry tetrahydrofuran while maintaining the temperature below -70° C. The mixture was stirred at -78° C. for 3 hours and dimethyl disulphide (60.65 g) was added. The mixture was allowed to warm to room temperature and stirred overnight. The mixture was evaporated to dryness and the residue was suspended in ether and washed with water, dried (MgSO4) and filtered. The filtrate was evaporated to dryness to give 2-chloro-6-fluorothioanisole (60 g) as a crude yellow oil containing some dimethyl disulphide, NMR (CDCl3) 2.45(s,3H), 6.95(t,1H), 7.1-7.3(m,2H).

Aufarbeitung

  1. temperaturewhile maintaining the temperature below -70° C
  2. temperatureto warm to room temperature
  3. stirringstirred overnight
  4. customThe mixture was evaporated to dryness
  5. washwashed with water
  6. dry with materialdried (MgSO4)
  7. filtrationfiltered
  8. customThe filtrate was evaporated to dryness

Quellen und Nachweise

ORD-Eintrag
ord-74d29cbdb4b64b6a9fac27f6d8a4488d
Quelldatensatz
uspto-grants-1999_01
Patentnummer
US05856274

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