Reaktion #367252

Reaktionsgleichung

methyl 2-mercapto-benzoate

chloromethyl 2,4-dichlorophenyl ether

→

1-(2,4-dichlorophenoxy)-1 -(2-methoxycarbonyl-phenylthio)-methane

Ausbeute 90.4%

Lösungsmittel

tetrahydrofuran

tetrahydrofuran

dimethylformamide

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.ADDITIONAt the end of the dropwise addition
2. 2
   SonstigeThe solid product precipitated
3. 3
   Filtrationwas filtered off with suction
4. 4
   workup.DISSOLUTIONdissolved in 100 ml of dimethylformamide
5. 5
   workup.STIRRINGwhile stirring at 25° C
6. 6
   workup.STIRRINGThe mixture was subsequently stirred at 30° C. for 1 hour
7. 7
   SonstigeThe suspension thereby formed
8. 8
   Filtrationwas filtered off with suction
9. 9
   Sonstigethe solid product precipitated
10. 10
    Sonstigewas dried in air

Vorschrift

A solution of 28 g (0.25 mol) of potassium tert.-butylate in 120 ml of tetrahydrofuran was slowly added dropwise to a solution of 33.6 g (0.2 mol) of methyl 2-mercapto-benzoate in 50 ml of tetrahydrofuran at 5° C. At the end of the dropwise addition, stirring was continued at 5° C. for a further 30 minutes. The solid product precipitated was filtered off with suction and dissolved in 100 ml of dimethylformamide. A solution of 42.3 g (0.2 mol) of chloromethyl 2,4-dichlorophenyl ether in 60 ml of dimethylformamide was added dropwise to this solution, while stirring at 25° C. The mixture was subsequently stirred at 30° C. for 1 hour and then worked up by stirring into 1.5 liters of ice-water. The suspension thereby formed was filtered off with suction and the solid product precipitated was dried in air. 62 g (90.4% of theory) of 1-(2,4-dichlorophenoxy)-1 -(2-methoxycarbonyl-phenylthio)-methane were obtained in this manner in the form of colourless crystals of melting point 122°-124° C.

Quelle