化工社化工社化学信息打印报告 · 仅供科研参考
三乙胺 → [2-(2-Hydroxy-ethoxy)-ethyl]-carbamic acid anthracen-9-ylmethyl ester
参与物
| 角色 | 名称 | HCID | 投料 |
|---|---|---|---|
| 反应物 | 三乙胺 | HCID 8471 | — |
| 反应物 | 二甘醇胺 | HCID 13578 | — |
| 反应物 | 9-蒽醇 | HCID 73848 | — |
| 反应物 | 对硝基苯基氯甲酸酯 | HCID 82129 | — |
| 催化剂 | Gold | HCID 23985 | — |
| 溶剂 | 二氯甲烷 | HCID 6344 | — |
| 产物 | [2-(2-Hydroxy-ethoxy)-ethyl]-carbamic acid anthracen-9-ylmethyl ester | HCID 10315131 | — |
反应步骤
To a stirring slurry of 9-anthracenemethanol (10 g, 48 mmol) and 4-nitrophenyl chloroformate (13.6 g, 67.5 mmol) in 200 ml CH2Cl2 was added triethylamine (6.7 ml, 0.19 mol). The resulting gold colored solution was allowed to stir 16 hrs at room temperature. At this point, 2-(2-aminoethoxy)ethanol (14.4 ml, 0.144 mol) was added and stirring continued for another 24 hours. The CH2Cl2 reaction mixture was then washed with a 2% sodium hydroxide (w/w) solution until no p-nitrophenol was observed in the organic layer. The dichloromethane was dried with sodium sulfate, filtered, and evaporated under reduced pressure.
来源与证据
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 专利号 | US07429472B2 |
| 来源数据集 | uspto-grants-2008_09 |
| ORD ID | ord-928dcbd36ef14c3e9a91d1edde5a98fa |
| 来源说明 | uspto-grants-2008_09 |