関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Myristyl bromide | HCID 8208 | — |
| 反応物 | 1,3-Propanediol | HCID 10442 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 溶媒 | dimethylsulfoxide THF | HCID 21830753 | — |
| 生成物 | 3-(Tetradecyloxy)propan-1-ol | HCID 114239 | 34.6% |
反応手順
In 70 ml of a mixture of dimethylsulfoxide-tetrahydrofuran (1:1) are dissolved 12.3 g of trimethylene glycol and 15 g of tetradecyl bromide. To the solution is added 12 g of powdery potassium hydroxide. The mixture is vigorously stirred for one hour at a room temperature, which is refluxed under heating for two hours. The reaction mixture is poured into 400 ml of cold water, which is neutralized and subjected to extraction with ethyl acetate, then washed with water and dried. The resultant is concentrated to dryness, and the residue is dissolved in methanol when hot. Cooling of the solution gives precipitation of crystals, which are removed by filtration. The filtrate is refined by means of chromatography employing silica-gel (eluent:chloroform) to give 5.1 g of the end-product.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US04544512 |
|---|
| 出典データセット | uspto-grants-1985_10 |
|---|
| ORD ID | ord-114af40f277c494d890493369382aa3d |
|---|
| 出典メモ | uspto-grants-1985_10 |
|---|