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HRID 128255作成日:2026年10月24日

Hydrochloric Acid → Sodium 2-carboxy-benzo[b]thiophene-3-sulfonate

https://huagongshe.com/ja/reaction/128255

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Sodium HydroxideHCID 14798—
反応物3-Chlorobenzo(b)thiophene-2-carbonyl chlorideHCID 519898—
反応物Sodium BisulfiteHCID 23665763—
触媒Cuprous chlorideHCID 62652—
溶媒WaterHCID 962—
生成物Sodium 2-carboxy-benzo[b]thiophene-3-sulfonateHCID 2371440548%

反応手順

74.0 gm (0.32 mol) of 3-chloro-benzo[b]thiophene-2-carboxylic acid chloride (m.p. 112°-113° C.) were stirred with a solution of 25.6 gm (0.64 mol) of sodium hydroxide in 250 cc of water for 12 hours while keeping the reaction temperature at 50° C. Thereafter 66.6 gm (0.64 mol) of solid sodium hydrogen sulfite were added to the neutral-reacting solution. The reaction mixture was made slightly alkaline by addition of a 40% sodium hydroxide solution and heated for 16 hours to 143° C. in an autoclave after addition of 3.0 gm (0.03 mol) of copper(I)-chloride. After cooling, the mixture was adjusted to pH 4 by adding hydrochloric acid, filtered and extracted once with 200 cc of ethyl acetate to remove the residual unreacted starting material. After further acidification to pH 1 and by addition of 60 gm of sodium chloride a colorless precipitate was obtained from the aqueous phase, which was suction-filtered off, washed with 30 cc of saturated aqueous sodium chloride solution and suction-filtered. The reaction product was dissolved in warm methanol and separated from the insoluble excess sodium chloride. The solvent was evaporated in vacuo, and the residue was dried by azeotropic distillation with 50 cc of toluene. 43 gm (48% of theory) of colorless crude sodium 2-carboxy-benzo[b]thiophene-3-sulfonate were obtained, which were further processed without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04259336
出典データセットuspto-grants-1981_03
ORD IDord-5b869c65d948469488ee3910faaec793
出典メモuspto-grants-1981_03