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HRID 745796作成日:2026年10月26日

Hydrochloric Acid → 5-(2-Chlorophenylsulphonyl)-6-methyl-1,3-benzodioxole-2-carboxylic acid

https://huagongshe.com/reaction/745796

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Potassium CarbonateHCID 11430—
反応物Dibromoacetic AcidHCID 12433—
反応物4-(2-Chlorophenylsulphonyl)-5-methyl-1,2-benzenediolHCID 23312099—
溶媒DimethylformamideHCID 6228—
生成物5-(2-Chlorophenylsulphonyl)-6-methyl-1,3-benzodioxole-2-carboxylic acidHCID 23312095—

反応手順

23 g (77 mmol) of 4-(2-chlorophenylsulphonyl)-5-methyl-1,2-benzenediol are added to a finely particulate suspension of 50.9 g (385 mmol) of freshly calcined potassium carbonate in 180 ml of dry dimethylformamide and there is added dropwise thereto, in the course of 15 minutes, a solution of 8.50 g (39 mmol) of dibromoacetic acid in 80 ml of dimethylformamide. The mixture is then stirred for 15 hours at 80°. Subsequently, the reaction mixture is poured onto ice and adjusted to pH 1-2 with concentrated hydrochloric acid. The aqueous phase is extracted once more with ethyl acetate. The combined organic phases are washed with water and saturated sodium chloride solution, dried with sodium sulphate and concentrated by evaporation. The resulting brown oil is stirred with 150 ml of ethyl acetate at 0° until crystallisation occurs. The crude 5-(2-chlorophenylsulphonyl)-6-methyl-1,3-benzodioxole-2-carboxylic acid so obtained is recrystallised twice from acetonitrile, resulting in the form of sand-coloured crystals having a melting point of 211°-213.5°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04600709
出典データセットuspto-grants-1986_07
ORD IDord-2bba5278dfe74136921fe1189a35daf6
出典メモuspto-grants-1986_07