p-Chlorothiophenol → HCID 10942819, compound

HRID 1165469Notes

Reaction equation

HRID 1165469 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([SH:8])=[CH:4][CH:3]=1.C[O-].[Na+:11]>CO>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([S-:8])=[CH:4][CH:3]=1.[Na+:11]

Participants

4

Conditions

Temperature
100 °C

Procedure

Sodium p-chlorothiophenoxide was prepared from p-chlorothiophenol (4.3 g) in methanol (10 ml) and sodium methoxide (5.4 g of a 30% sodium methoxide solution) by evaporation in a rotary evaporator. The resulting salt was dissolved, together with 3,4-dimethoxy-4'-fluorobenzophenone (7.8 g) in dimethylformamide (30 ml), and the solution was heated at 100° C. for 3 hours. Then, the reaction mixture was poured into water, and the crystals which precipitated were recrystallized from ethanol.

Workup

  1. customby evaporation
  2. customin a rotary evaporator
  3. dissolutionThe resulting salt was dissolved, together with 3,4-dimethoxy-4'-fluorobenzophenone (7.8 g) in dimethylformamide (30 ml)
  4. additionThen, the reaction mixture was poured into water
  5. customthe crystals which precipitated
  6. customwere recrystallized from ethanol

Sources & evidence

ORD record
ord-31208f6518ec414e801a72b40185193b
Source dataset
uspto-grants-1990_03
Patent number
US04910200

Reaction notes

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