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[2-(2-Chlorobenzyloxy)phenyl]methanol → [2-(2-Chlorobenzyloxy)benzyl]triphenylphosphonium bromide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | [2-(2-Chlorobenzyloxy)phenyl]methanol | HCID 961592 | — |
| 反応物 | Triphenylphosphonium hydrobromide | HCID 22178555 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | [2-(2-Chlorobenzyloxy)benzyl]triphenylphosphonium bromide | HCID 86634293 | 99.7% |
反応手順
A solution of 3.775 g (15.18 mmol) of [2-(2-chlorobenzyloxy)phenyl]methanol from Example 78A in 60 ml of acetonitrile is mixed with 4.949 g (14.42 mmol) of triphenylphosphonium hydrobromide and heated to reflux for 3 hours. The reaction solution is then concentrated to dryness, and the resulting oil is taken up and triturated in diethyl ether. The product crystallizes as a white solid during this. After filtration, the solid is dried in a drying oven at 50° C. overnight. 8.247 g (91% yield) of crystalline product are obtained.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07998988B2 |
| 出典データセット | uspto-grants-2011_08 |
| ORD ID | ord-be153121de4f47eaaac75249dbc3d6fc |
| 出典メモ | uspto-grants-2011_08 |