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Hydrochloric Acid → 4-(Hydroxymethyl)-4-piperidinol hydrochloride
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | 1-Benzyl-4-(hydroxymethyl)piperidin-4-ol | HCID 14025336 | — |
| 触媒 | HCID 178418390 | HCID 178418390 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 4-(Hydroxymethyl)-4-piperidinol hydrochloride | HCID 22744472 | — |
反応手順
500 mg of 1-benzyl-4-(hydroxymethyl)piperidin-4-ol (synthesized according to the method described in J. Med. Chem., 1988, 486-491) was dissolved in 10 ml of ethanol, 300 mg of 10% palladium carbon and 0.38 ml of concentrated hydrochloric acid were added thereto, and the mixture was subjected to hydrogenation at room temperature overnight. The reaction mixture was filtrated to remove precipitates, the precipitates were washed with ethanol and water, and the filtrate was concentrated under reduced pressure. The obtained residue was turned into powder by adding diethylether to obtain 374 mg of the objective compound as a white powder.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08586591B2 |
| 出典データセット | uspto-grants-2013_11 |
| ORD ID | ord-4e510fa01fb14463a48738b2380e3fd0 |
| 出典メモ | uspto-grants-2013_11 |