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HRID 982465作成日:2026年10月25日
Hydrochloric Acid → 1-(3-Methylthio-4-propoxy-5-benzyloxyphenyl)4-(3,4,5-trimethoxyphenyl)butan-1,4-dione
https://huagongshe.com/reaction/982465
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 1,5-Bis(3,4,5-trimethoxyphenyl)penta-1,4-dien-3-one | HCID 383405 | — |
| 反応物 | 3-Methylthio4-n-propoxy-5-benzyloxybenzaldehyde | HCID 10471022 | — |
| 触媒 | 3-Ethyl-5-(2-hydroxyethyl)-4-methylthiazolium bromide | HCID 9964923 | — |
| 生成物 | 1-(3-Methylthio-4-propoxy-5-benzyloxyphenyl)4-(3,4,5-trimethoxyphenyl)butan-1,4-dione | HCID 10098743 | — |
反応手順
175 g 3-methylthio-4-n-propoxy-5-benzyloxybenzaldehyde, 135 g of 3,4,5-trimethoxyphenylvinylketone, 10 g of 3-ethyl-5-(2-hydroxyethyl)-4-methylthiazoliumbromide, 25 mL of triethyl amine dissolved in 150 ml of dimethylformamide was heated at 60° C. overnight, and the reaction mixture was treated with 400 mL of 1.5N HCl and the aqueous layer decanted. The residue was treated again with fresh 400 mL of 1.5N HCl and decanted two more times. The remaining residue was crystallized from 400 mL of methanol and washed thoroughly with methanol, hexane, and methanol and dried to yield the title compound as a tan solid: NMR(200 MHz, CDCl3) δ 1.03(t, CH2CH2CH3), 1.82(m, CH2CH2CH3), 2.50(s, SCH3), 3.43(s, C(O)CH2CH2CO), 3.94(s, 3 OCH3), 4.11(t, OCH2CH2CH3), 5.17(s, OCH2Ar), 7.30-7.52(m, ArH).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04996203 |
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| 出典データセット | uspto-grants-1991_02 |
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| ORD ID | ord-6281e817a89f44aa85263744adfdab80 |
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| 出典メモ | uspto-grants-1991_02 |
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