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HRID 1736334作成日:2026年10月25日

Hydrochloric Acid → HCID 178468679、化合物

https://huagongshe.com/reaction/1736334

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BenzothiazoleHCID 7222—
反応物Ethyl 2-bromo-6-benzothiazolecarboxylateHCID 12067225—
反応物Potassium hydrogensulfideHCID 86743134—
溶媒EthanolHCID 702—
生成物HCID 178468679HCID 178468679—

反応条件

温度80 °C

反応手順

The crude 2-bromo-6-ethoxycarbonylbenzothiazole (1.90 g, 6.64 mmol) from Step 2 was suspended in absolute ethanol (35 mL) and treated with potassium hydrogen sulfide (0.96 g, 13.3 mmol). The mixture was placed under a nitrogen atmosphere, stirred, and heated in an oil bath at 80° C. The benzothiazole starting material gradually went into solution. After heating for 30 minutes, the mixture was cooled in an ice bath, treated with 1N hydrochloric acid (13.5 mL), and evaporated under vacuum. The residue was partitioned between ethyl acetate (100 mL) and water (100 mL) and the aqueous phase extracted with more ethyl acetate (50 mL). The combined ethyl acetate solution was washed with brine (50 mL), dried over sodium sulfate, filtered and evaporated under vacuum to a yellow-tan solid (1.56 g). This material was triturated with diethyl ether and dried under vacuum to provide 6-ethoxycarbonyl-2-mercaptobenzothiazole (1.14 g) as a pale tan powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05541176
出典データセットuspto-grants-1996_07
ORD IDord-b498c746710d48439f77756165ea961a
出典メモuspto-grants-1996_07