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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 745796생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/745796

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Potassium CarbonateHCID 11430—
반응물Dibromoacetic AcidHCID 12433—
반응물4-(2-Chlorophenylsulphonyl)-5-methyl-1,2-benzenediolHCID 23312099—
용매DimethylformamideHCID 6228—
생성물5-(2-Chlorophenylsulphonyl)-6-methyl-1,3-benzodioxole-2-carboxylic acidHCID 23312095—

반응 단계

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°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04600709
출처 데이터셋uspto-grants-1986_07
ORD IDord-2bba5278dfe74136921fe1189a35daf6
출처 메모uspto-grants-1986_07