p-Chlorothiophenol → HCID 10942819, compound
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
Reactant 2
Product 1
Reagents, catalysts & solvents 1
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
- customby evaporation
- customin a rotary evaporator
- dissolutionThe resulting salt was dissolved, together with 3,4-dimethoxy-4'-fluorobenzophenone (7.8 g) in dimethylformamide (30 ml)
- additionThen, the reaction mixture was poured into water
- customthe crystals which precipitated
- 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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