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HRID 280070作成日:2026年10月27日

Benzoic acid, 2-mercapto-, methyl ester → 1-(2,4-Dichlorophenoxy)-1-(2-methoxycarbonyl-phenylthio)-methane

https://huagongshe.com/reaction/280070

反応式

関与物質

役割名称HCID仕込み量
反応物Benzoic acid, 2-mercapto-, methyl esterHCID 21009—
反応物Chloromethyl 2,4-dichlorophenyl etherHCID 12353529—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
生成物1-(2,4-Dichlorophenoxy)-1-(2-methoxycarbonyl-phenylthio)-methaneHCID 1559196890.4%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04588433
出典データセットuspto-grants-1986_05
ORD IDord-7fb8992cf57545959c29c1891f75bff4
出典メモuspto-grants-1986_05