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HRID 552281作成日:2026年10月27日
1-(5-Ethyl-4-phenyl-thiophen-2-yl)-ethanone → 3-[4-(2,3-Dihydroxy-propyl)-3,5-dimethyl-phenyl]-1-(5-ethyl-4-phenyl-thiophen-2-yl)-propan-1-one
https://huagongshe.com/reaction/552281
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 1-(5-Ethyl-4-phenyl-thiophen-2-yl)-ethanone | HCID 67166164 | — |
| 反応物 | 4-(2,3-Dihydroxy-propyl)-3,5-dimethyl-benzaldehyde | HCID 86640171 | — |
| 溶媒 | Hydrochloric Acid | HCID 313 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Isopropanol | HCID 3776 | — |
| 生成物 | 3-[4-(2,3-Dihydroxy-propyl)-3,5-dimethyl-phenyl]-1-(5-ethyl-4-phenyl-thiophen-2-yl)-propan-1-one | HCID 59249000 | 21.7% |
反応手順
A solution of 4-(2,3-dihydroxy-propyl)-3,5-dimethyl-benzaldehyde (64 mg, 0.308 mmol) and 1-(5-ethyl-4-phenyl-thiophen-2-yl)-ethanone (50 mg, 0.218 mmol) in ethanol (2 mL) and 5 N HCl in isopropanol (0.5 mL) is stirred at rt for 5 days. The solvent is removed in vacuo and the residue is separated by prep. HPLC. Product containing fractions are treated with sat. aq. NaHCO3 and 3 M aq. NaOH (5 mL). The mixture is stirred at rt for 1 h, then extracted with DCM. The solvent of the organic extract is removed. The residue is dissolved in THF:methanol 1:1 (5 mL) and is treated with Pd/C. The slurry is stirred at it for 16 h under 1.5 bar of H2. The mixture is filtered over celite and the filtrate is evaporated to give 3-[4-(2,3-dihydroxy-propyl)-3,5-dimethyl-phenyl]-1-(5-ethyl-4-phenyl-thiophen-2-yl)-propan-1-one (20 mg) as a colourless oil, LC-MS: tR=1.04 min, [M+1]+=423.28.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07951794B2 |
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| 出典データセット | uspto-grants-2011_05 |
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| ORD ID | ord-0ffae9ba1c224dfe8a50ca4d95f8de6a |
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| 出典メモ | uspto-grants-2011_05 |
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