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(+-)-4-Hydroxymandelic acid → p-Nitrobenzyl 4-hydroxymandelate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | (+-)-4-Hydroxymandelic acid | HCID 328 | — |
| 反応物 | Dimethylacetamide | HCID 31374 | — |
| 反応物 | 4-Nitrobenzyl bromide | HCID 66011 | — |
| 反応物 | Potassium tert-butoxide | HCID 23665647 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | p-Nitrobenzyl 4-hydroxymandelate | HCID 13066460 | 84% |
反応手順
To a solution of 16.8 g. (0.1 mole) of 4-hydroxymandelic acid in 300 ml. of dimethylacetamide were added 11.2 g. of potassium t-butoxide with an additional 100 ml. of dimethylacetamide. The mixture was stirred at room temperature until a solution was obtained. p-Nitrobenzyl bromide (21.6 g., 0.1 mole) was added to the solution followed by 100 ml. of additional dimethylacetamide. The reaction mixture was stirred for 24 hours and was diluted with one liter of ethyl acetate. The mixture was washed repeatedly with water and dried over magnesium sulfate. The dried solution was evaporated to yield 25 g. (84 percent yield) of p-nitrobenzyl 4-hydroxymandelate.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04355172 |
| 出典データセット | uspto-grants-1982_10 |
| ORD ID | ord-97b1b52820544c818657c0ef02c23237 |
| 出典メモ | uspto-grants-1982_10 |