化工社化工社 化学情報印刷レポート · 研究参考用
N-methyl-2-pyrrolidone → 2,4,8,10-Tetra-tert-butyl-6-chloro-12-methyl-12H-dibenzo[d,g][1,3,2]dioxaphosphocine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 反応物 | Phosphorus trichloride | HCID 24387 | — |
| 反応物 | 2,2'-Ethylidenebis(4,6-di-tert-butylphenol) | HCID 118899 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 2,4,8,10-Tetra-tert-butyl-6-chloro-12-methyl-12H-dibenzo[d,g][1,3,2]dioxaphosphocine | HCID 11060203 | 34.8% |
反応手順
To a solution of 50.9 g. (0.12 mol) of 2,2'-ethylidenebis(4,6-di-tert-butylphenol) and 1.73 mL (0.018 mol) of 1-methyl-2-pyrrolidinone in 275 mL of toluene at ambient temperature is added dropwise 15.7 mL (0.18 mol) of phosphorus trichloride. After the addition is complete, the reaction mixture is heated at reflux for 18 hours. After cooling to room temperature, the toluene is removed in vacuo and the residue is then recrystallized twice from 250 mL of acetonitrile. The acetonitrile is decanted from the product which is dried under vacuum to give 21.0 g (34.8% yield) of the title compound as an off-white solid melting at 194°-198° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05475042 |
| 出典データセット | uspto-grants-1995_12 |
| ORD ID | ord-63b22777b23f4ce08ef791f2733bb9d5 |
| 出典メモ | uspto-grants-1995_12 |