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Potassium Hydroxide → (E)-3-(4-{(E)-3-[4-(1-methyl-piperidin-4-yl)-phenyl]-3-oxo-propenyl}-phenyl)-acrylic acid tert-butyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | 4-Formylcinnamic acid tert-butyl ester | HCID 54147604 | — |
| 反応物 | 1-(4-(1-Methylpiperidin-4-yl)phenyl)ethan-1-one hydrochloride | HCID 67049733 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | (E)-3-(4-{(E)-3-[4-(1-methyl-piperidin-4-yl)-phenyl]-3-oxo-propenyl}-phenyl)-acrylic acid tert-butyl ester | HCID 67049486 | 29.1% |
反応手順
A mixture of 1-[4-(1-methyl-piperidin-4-yl)-phenyl]-ethanone hydrochloride (544 mg, 2.15 mmol), 4-formylcinnamic acid tert-butyl ester (500 mg, 2.15 mmol) and 1.7 M KOH (3.8 ml, 6.46 mmol) in EtOH (10 ml) was stirred at room temperature for 6 hours. During the reaction, the formation of a precipitate was observed. The solid was then filtered off through a Buchner funnel to obtain 270 mg of (E)-3-(4-{(E)-3-[4-(1-methyl-piperidin-4-yl)-phenyl]-3-oxo-propenyl}-phenyl)-acrylic acid tert-butyl ester as a yellow solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08242175B2 |
| 出典データセット | uspto-grants-2012_08 |
| ORD ID | ord-2125cb7bae3943d9bbf74a534e66d532 |
| 出典メモ | uspto-grants-2012_08 |