참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethanol | HCID 702 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | 2-Acetyl-4,5-dihydro-6,8-dimethylnaphtho[1,2-b]thiophene | HCID 11172895 | — |
| 반응물 | HCID 178418435 | HCID 178418435 | — |
| 생성물 | 2-(2-Hydroxyethyl)-4,5-dihydro-6,8-dimethylnaphtho[1,2-b]thiophene | HCID 23117351 | — |
반응 단계
0.18 g of sodium boron hydride was added under nitrogen replacement and ice cooling to a 10 mL ethanol solution of 0.50 g of the compound obtained in Example 1, and the system was stirred for 2 hours at room temperature. After the reaction, reduced-pressure solvent distillation was performed, a saturated ammonium chloride aqueous solution was added under ice cooling, extraction was performed with ethyl acetate, and the organic layer was washed with saturated brine, dried with magnesium sulfate, and then subjected to reduced-pressure solvent distillation, and the residue was refined by silica gel column chromatography (25% ethyl acetate/hexane) to obtain 0.50 g of 2-(2-hydroxyethyl)-4,5-dihydro-6,8-dimethylnaphtho[1,2-b]thiophene (Table 9-1) in the form of a brown solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07384974B2 |
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| 출처 데이터셋 | uspto-grants-2008_06 |
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| ORD ID | ord-e3b5a964cd8a4940b83478373bd39f6f |
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| 출처 메모 | uspto-grants-2008_06 |
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