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(5-Carboxypentyl)triphenylphosphanium bromide → 14-Hydroxy-7-methyl-pentadec-6-enoic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | (5-Carboxypentyl)triphenylphosphanium bromide | HCID 2779280 | — |
| 反応物 | 9-Hydroxy-2-decanone | HCID 21187407 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 14-Hydroxy-7-methyl-pentadec-6-enoic acid | HCID 73753002 | 98.3% |
反応手順
325 g (0.7 mol) of (5-carboxypentyl)triphenylphosphonium bromide were dissolved in 1500 ml of tetrahydrofuran. After the addition of 180 g (1.6 mol) of potassium t-butylate in 700 ml of tetrahydrofuran the mixture was treated with 175 g (0.71 mol) of 9-hydroxy-2-decanone (70% purity). After usual work up 186 g of crude 14-hydroxy-7-methyl-pentadec-6-enoic acid were obtained. This product was dissolved in 400 ml of methanol and, after the addition of 5 ml of concentrated sulphuric acid, heated to reflux for 2 hours. After work up, bulb-tube distillation and chromatography 102 g (50%) of methyl 14-hydroxy-7-methyl- pentadec-6-enoate were obtained having the following characteristics:
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06255276B1 |
| 出典データセット | uspto-grants-2001_07 |
| ORD ID | ord-bc42591867964792bde017d4e9f14f30 |
| 出典メモ | uspto-grants-2001_07 |