関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Trimesoyl chloride | HCID 78138 | — |
| 反応物 | HCID 178420729 | HCID 178420729 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | 1,3,5-Tris-(5-[1,10]phenanthroline-2-yl-[1,3,4]oxadiazol-2-yl)-benzene | HCID 58979968 | 44.1% |
反応手順
To a flask was added a mixture of 15 g 2-(1H-tetrazol-5-yl)-[1,10]phenanthroline and 300 ml pyridine. The mixture was then heated to 80-90° C., and 4.86 g 1,3,5 benzene tricarbonyl chloride was added. Subsequently, the mixture solution was heated to 110° C. and stirred overnight. After completion of reaction, as shown in scheme 8, the reaction mixture was filtered to collect solids. The solids was washed by pyridine and CH2Cl2 respectively, and then dried on oven to obtain products 6.6 g (yield=44.1%). MS(m/z, FAB+), 888, 810, 521, 444, 155.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US07282586B1 |
|---|
| 出典データセット | uspto-grants-2007_10 |
|---|
| ORD ID | ord-42c58dc405e44091894b97aeb08b019a |
|---|
| 出典メモ | uspto-grants-2007_10 |
|---|