関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | 1-Hydroxy-4-benzoyloxy-2,2,6,6-tetramethylpiperidine | HCID 688178 | — |
| 反応物 | Potassium cyanate | HCID 11378442 | — |
| 反応物 | HCID 178513472 | HCID 178513472 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 1-Carbamoyloxy-4-benzoyloxy-2,2,6,6-tetramethylpiperidine | HCID 19090576 | 81% |
反応手順
A solution of 6.7 ml of 12 N HCl in 10 ml of water is added dropwise over 10 minutes with cooling below 0° C. to a suspension of 20.8 g (75 mmol) of 1-hydroxy-4-benzoyloxy-2,2,6,6-tetramethylpiperidine, 75 ml of methanol, and 25 ml of water in a nitrogen atmosphere. A clear solution resulted. A solution of 6.1 g (75 mmol) of potassium cyanate in 25 ml of water is added dropwise over 30 minutes. The reaction temperature is maintained at 0-5° C. during the cyanate addition. The reaction mixture is stirred 30 minutes at ambient temperature, then filtered. The precipitate is washed with water, then dissolved in 200 ml of toluene. Residual water is removed by azeotropic distillation. The toluene solution is then cooled to yield 19.4 g (81%) of a white crystalline solid, m.p. 148-49° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US05300647 |
|---|
| 出典データセット | uspto-grants-1994_04 |
|---|
| ORD ID | ord-fd3396c6288947c492ab1d4e064a036a |
|---|
| 出典メモ | uspto-grants-1994_04 |
|---|