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p-Toluenesulfonic acid → Benzyl [2-(4-benzhydrylpiperidino)-2-oxoethoxy]acetate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | p-Toluenesulfonic acid | HCID 6101 | — |
| 反応物 | Mcn 4308 | HCID 196442 | — |
| 溶媒 | Benzyl Alcohol | HCID 244 | — |
| 生成物 | Benzyl [2-(4-benzhydrylpiperidino)-2-oxoethoxy]acetate | HCID 54337918 | — |
反応手順
In a similar operation, 3.63 grams (10 millimoles) of [2-(4-benzhydrylpiperidino)-2-oxoethoxy]acetic acid, 50 milliliters of benzyl alcohol and 150 milligrams of p-toluenesulfonic acid are mixed together and the resulting mixture heated at reflux temperature for about 6 hours to obtain a product in the reaction mixture. Thereafter, the reaction mixture subjected to reduced pressure to evaporate the alcohol and the residue is dissolved in benzene, the resulting solution washed with bicarbonate solution, dried and the solvent evaporated to obtain a benzyl [2-(4-benzhydrylpiperidino)-2-oxoethoxy]acetate product. The molecular weight of benzyl [2-(4-benzhydrylpiperidino)-2-oxoethoxy]acetate is 453.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04203991 |
| 出典データセット | uspto-grants-1980_05 |
| ORD ID | ord-f2d81979881a46fe8cff0aac2c8f1a3c |
| 出典メモ | uspto-grants-1980_05 |