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1,2,2,6,6-Pentamethyl-4-piperidone → 1,2,2,4,6,6-Hexamethylpiperidin-4-ol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1,2,2,6,6-Pentamethyl-4-piperidone | HCID 241955 | — |
| 反応物 | HCID 178418348 | HCID 178418348 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | 1,2,2,4,6,6-Hexamethylpiperidin-4-ol | HCID 434568 | 91.8% |
反応手順
To a stirred solution of 1,2,2,6,6-pentamethylpiperidin-4-one (1.5 g, 8.88 mmol) in diethyl ether (25 mL) at rt was added MeLi (1.6 M, 5.5 mL, 8.88 mmol) slowly. The resulting mixture was stirred at rt for 30 min before it was quenched with sat. NH4Cl (15 mL). The mixture was then partitioned between EtOAc (35 mL) and sat. NaHCO3 (25 mL). The organic layer was dried over Na2SO4, filtered, and concentrated under reduced pressure to give crude 1,2,2,4,6,6-hexamethylpiperidin-4-ol (1.51 g) as an oil. LC-MS (ESI) m/z 186 (M+H)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09296722B2 |
| 出典データセット | uspto-grants-2016_03 |
| ORD ID | ord-ea26526e8fa845b3913bf6b5c67a73ea |
| 出典メモ | uspto-grants-2016_03 |