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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 413585생성일: 2026년 10월 25일

Hydrochloric Acid → Ethyl 7-(4-ethoxyphenyl)-2,3-dihydro-1-benzothiepine-4-carboxylate

https://huagongshe.com/reaction/413585

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Diethyl CarbonateHCID 7766—
반응물Potassium CarbonateHCID 11430—
반응물Ethyl 4-sulfanylbutanoateHCID 271824—
반응물Sodium ethoxideHCID 2723922—
반응물5-(4-Ethoxyphenyl)-2-fluorobenzaldehydeHCID 18533382—
용매EthanolHCID 702—
용매IsopropanolHCID 3776—
용매DimethylformamideHCID 6228—
생성물Ethyl 7-(4-ethoxyphenyl)-2,3-dihydro-1-benzothiepine-4-carboxylateHCID 1853338757%

반응 단계

Under an argon atmosphere, 5-(4-ethoxyphenyl)-2-fluorobenzaldehyde (1.0 g) was dissolved in 2 ml of dimethylformamide and 1.17 g of potassium carbonate was added. Thereafter, 1.18 ml of ethyl 4-mercaptobutyrate was added and was stirred at room temperature for 25 hours. After addition of 20 ml of diethyl carbonate and an ethanol solution (2.8 g) of 20% sodium ethoxide, stirring was conducted at room temperature for three hours. During cooling in ice, 21 ml of a 1N hydrochloric acid was added. The mixture was extracted with 50 ml and additional 20 ml of ethyl acetate. The organic layers were combined and washed with 20 ml of water twice. The resulting organic layer was concentrated to yield crystals, which crystals were loosen in 2 ml of isopropyl alcohol added. The crystals were filtered out and were washed with 4 ml of isopropyl ether twice. After vacuum drying, ethyl 7-(4-ethoxyphenyl)-2,3-dihydro-1-benzothiepine-4-carboxylate (0.8 g, Yield 57%) was obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06566535B1
출처 데이터셋uspto-grants-2003_05
ORD IDord-e534bfe1a2104df69ebe53303b61702e
출처 메모uspto-grants-2003_05