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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1735716생성일: 2026년 10월 25일

Hydrochloric Acid → HCID 178468679, 화합물

https://huagongshe.com/reaction/1735716

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물BenzothiazoleHCID 7222—
반응물Ethyl 2-bromo-6-benzothiazolecarboxylateHCID 12067225—
반응물Potassium hydrogensulfideHCID 86743134—
용매EthanolHCID 702—
생성물HCID 178468679HCID 178468679—

반응 조건

온도80 °C

반응 단계

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 starring material gradually went into solution. After hearing 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05538964
출처 데이터셋uspto-grants-1996_07
ORD IDord-7098db7632f847ec9dacbaa9ba87094d
출처 메모uspto-grants-1996_07