참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Diethyl Carbonate | HCID 7766 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Ethyl 4-sulfanylbutanoate | HCID 271824 | — |
| 반응물 | Sodium ethoxide | HCID 2723922 | — |
| 반응물 | 5-(4-Ethoxyphenyl)-2-fluorobenzaldehyde | HCID 18533382 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Isopropanol | HCID 3776 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | Ethyl 7-(4-ethoxyphenyl)-2,3-dihydro-1-benzothiepine-4-carboxylate | HCID 18533387 | 57% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06566535B1 |
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| 출처 데이터셋 | uspto-grants-2003_05 |
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| ORD ID | ord-e534bfe1a2104df69ebe53303b61702e |
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| 출처 메모 | uspto-grants-2003_05 |
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