関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Benzyl Bromide | HCID 7498 | — |
| 反応物 | 5-Methyl-3-phenylisoxazole-4-carboxylic acid | HCID 14343 | — |
| 反応物 | Lithium | HCID 3028194 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Hexane | HCID 8058 | — |
| 生成物 | 3-Phenyl-5-(2-phenylethyl)isoxazole-4-carboxylic acid | HCID 23447906 | 84% |
反応手順
To a solution of 1.5 g of 5-methyl-3-phenyl-4-isoxazolecarboxylic acid in 50 mL of anhydrous tetrahydrofuran stirred at −78 ° C. under N2 atmosphere, 5.9 mL of a 2.5M solution of n-buthyl lithium in n-hexane was added and the solution was stirred at −78° C. for 2 hours. Afterwards, 0.89 mL of benzyl bromide was added at −78° C. and the solution stirred at room temperature for 2 hours. After overnight resting, the solution was poured into water (300 mL), acidified with hydrochloric acid and extracted with ethyl acetate (2×200 mL). The combined organic layers were washed with water, dried (sodium sulphate) and the solvents were evaporated to dryness. The solid residue was washed with petroleum ether to give 1.82 g (84%) of the title compound as an amorphous solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06365591B1 |
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| 出典データセット | uspto-grants-2002_04 |
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| ORD ID | ord-24fd1e98a5f84dc5aa4538b128321716 |
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| 出典メモ | uspto-grants-2002_04 |
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