참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Nitric Acid | HCID 944 | — |
| 반응물 | 4,5,6,7-Tetrahydro-4-oxothionaphthene | HCID 83418 | — |
| 용매 | Sulfuric Acid | HCID 1118 | — |
| 생성물 | 2-nitro-6,7-dihydrobenzo[b]thiophen-4(5H)-one | HCID 762878 | 75% |
반응 단계
was prepared using a literature procedure (Asprou et al., J. Heterocyclic Chem., 17:87-92 (1980) (“Asprou”), which is hereby incorporated by reference). To a 50 mL round bottom flask charged with a stir bar was added 4-keto-4,5,6,7-tetrahydrothianaphthene (0.61 g, 4 mmole) and concentrated sulfuric acid (6 mL). The solution was then cooled in an ice/salt bath to −5° C. and stirred while a solution of concentrated nitric acid (0.3 mL) in concentrated sulfuric acid (3 mL) was added dropwise over 30 minutes. Solution was stirred for another 50 minutes and allowed to gradually warm to 5° C. The reaction mixture was then poured onto crushed ice and the yellow precipitate filter and washed with several portions of ice-cold water to give product as a yellow solid (0.594 g, 75% yield). Spectral data were consistent with the literature values (Asprou, which is hereby incorporated by reference).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07816536B2 |
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| 출처 데이터셋 | uspto-grants-2010_10 |
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| ORD ID | ord-b272368ffc8a43ddbb994ff37ccc0143 |
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| 출처 메모 | uspto-grants-2010_10 |
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