関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Phosphate | HCID 1061 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Sodium Sulfate | HCID 24436 | — |
| 反応物 | 4-Benzyloxy-1-butanol | HCID 562212 | — |
| 反応物 | Sodium Hypochlorite | HCID 23665760 | — |
| 反応物 | Sodium Chlorite | HCID 23668197 | — |
| 触媒 | Tempo | HCID 2724126 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 4-(Benzyloxy)butanoic acid | HCID 562201 | 102% |
反応手順
3.0 g of 4-benyloxybutanol and 182 mg of TEMPO (2,2,6,6-tetramethyl-1-piperidinyloxy, radical) were dissolved in a mixture composed of 60 ml of acetonitrile and 60 ml of phosphate buffer (pH 6.7). To this reaction mixture were added 20 ml of an aqueous solution of sodium chlorite (NaClO2) (3.8 g) and 0.5 ml of a 5% aqueous solution of sodium hypochlorite (NaClO), followed by stirring at 35° C. for 5.5 hours. The reaction mixture was adjusted to pH 8.0 by the addition of a 2M aqueous solution of sodium hydroxide, and stirred for 20 minutes. Thereafter, 84 ml of an aqueous solution of sodium sulfate (5.1 g) was added thereto under cooling with ice so that its internal temperature would not exceed 20° C., followed by stirring for 30 minutes. After the reaction mixture was washed with 50 ml of t-butylmethyl ether, the aqueous solution was adjusted to pH 3-4 by the addition of 1M hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed with water and then with a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to obtain 3.3 g (102% yield) of the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06667325B1 |
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| 出典データセット | uspto-grants-2003_12 |
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| ORD ID | ord-bcb12d447c5142bfb0ae99809ba910cf |
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| 出典メモ | uspto-grants-2003_12 |
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