化工社化工社 化学情報印刷レポート · 研究参考用
Ammonium Chloride → 3-Methoxymethyloxy-1,2-benzenedimethanol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | Aluminium lithium hydride | HCID 21226445 | — |
| 反応物 | 3-Methoxymethyloxyphthalic anhydride | HCID 21936735 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 3-Methoxymethyloxy-1,2-benzenedimethanol | HCID 22272852 | 60% |
反応手順
After that, lithium aluminum hydride (1.14 g, 30.0 mmol) was added little by little to a solution of 3-methoxymethyloxyphthalic anhydride (3.0 g, 14.4 mmol) in anhydrous tetrahydrofuran (100 ml) under cooling with ice water and the mixture was returned to room temperature followed by stirring for 12 hours. The reaction solution was diluted with ether (300 ml) and a saturated aqueous solution (3 ml) of ammonium chloride was added thereto followed by stirring for 1 hour. The reaction solution was dried over anhydrous magnesium sulfate, filtered off through celite and the filtrate was concentrated to provide 1.71 g (yield 60%) of 3-methoxymethyloxy-1,2-benzenedimethanol as colorless oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06969711B2 |
| 出典データセット | uspto-grants-2005_11 |
| ORD ID | ord-643fbb12b6c24edf9251de60c65dea63 |
| 出典メモ | uspto-grants-2005_11 |