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Methyl p-toluenesulfonate → HCID 86744275、化合物
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methyl p-toluenesulfonate | HCID 6645 | — |
| 反応物 | 2-Propen-1-ol, 3-(3-pyridinyl)- | HCID 3563504 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 生成物 | HCID 86744275 | HCID 86744275 | — |
反応手順
Ethyl 3-(3-pyridyl)acrylate was reduced using lithium aluminum hydride to give 3-(3-pyridyl)-2-propen-1-ol. In 30 ml of acetone 710 mg of 3-(3-pyridyl)-2-propen-1-ol and 980 mg of methyl p-toluenesulfonate were heated under reflux for 22 hours. The reaction mixture was subjected by decantation to remove the solvent and then washed with acetone and ether. The residue was dried under reduced pressure to give 1.3 g of the desired compound as an orange-colored oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04962096 |
| 出典データセット | uspto-grants-1990_10 |
| ORD ID | ord-ab0bd96f038e4c9a91427c8f4d4a31c1 |
| 出典メモ | uspto-grants-1990_10 |