化工社化工社 化学情報印刷レポート · 研究参考用
3-Octanol → 1,3-Bis[N-n-octyl-N-(2,2,6,6-tetramethyl-4-piperidyl)amino]cyclobutenediylium-2,4-diolate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3-Octanol | HCID 11527 | — |
| 反応物 | Squaric acid | HCID 17913 | — |
| 反応物 | 2,2,6,6-Tetramethyl-4-octylaminopiperidine | HCID 14365121 | — |
| 溶媒 | Cyclohexane | HCID 8078 | — |
| 生成物 | 1,3-Bis[N-n-octyl-N-(2,2,6,6-tetramethyl-4-piperidyl)amino]cyclobutenediylium-2,4-diolate | HCID 178443594 | 84.4% |
反応手順
Under agitation, 339.6 g (1.26 moles) of 99.4% strength 4-n-octylamino-2,2,6,6-tetramethylpiperidine, 7.2 g (0.063 mole) of quadratic acid, and 150 cc of ethylhexanol was heated to boiling with reflux for 2.5 hours in a 1-liter stirred flask with water trap attached thereto; the solid matter was dissolved even before reaching reflux above 150° C. The sump temperature was 220° C. The amount of water removed from the cycle was 2.2 cc. Crystals precipitated from the reaction solution. After washing with petroleum ether and drying, 25.8 g was obtained. Yield: 84.4% of theory, mp 171°-175° C. (from cyclohexane). Extinction (g/l.cm) at 278 nm: 21; at 335 nm: 77.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04537924 |
| 出典データセット | uspto-grants-1985_08 |
| ORD ID | ord-cb9a5b0bd4ec4d619ed123b902c0d11c |
| 出典メモ | uspto-grants-1985_08 |