関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Diethyl Ether | HCID 3283 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | 4-Iodomethyl-5-methyl-2-m-tolyloxazole | HCID 21980308 | — |
| 反応物 | cis-3-Allylcyclohexanol | HCID 58763359 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 4-(cis-3-Allylcyclohexyloxymethyl)-2-(3-methylphenyl)-5-methyloxazole | HCID 68857183 | — |
反応手順
2 g of cis-3-allylcyclohexanol are dissolved in 30 ml of dimethylformamide, and 750 mg of sodium hydride (60% strength suspension in paraffin oil) are added. After 30 minutes, 6.7 g of 4-iodomethyl-5-methyl-2-(3-methylphenyl)oxazole, dissolved in 20 ml of dimethylformamide, are added dropwise. The mixture is stirred at room temperature for 1 hour. 200 ml of methy tert-buthyl ether are then added to the reaction mixture, and the mixture is washed three times with water. The organic phase is dried over magnesium sulfate and the solvent is then removed under reduced pressure. The residue is purified by RP-HPLC. This gives 1.56 g of 4-(cis-3-allylcyclohexyloxymethyl)-2-(3-methylphenyl)-5-methyloxazole as an oil. C21H27NO2 (325.45), MS (ESI): 326 (M+H+), Rf(n-heptane:ethylacetate=2:1)=0.28.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07148246B2 |
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| 出典データセット | uspto-grants-2006_12 |
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| ORD ID | ord-1ea7bf2aa6d04216be5e39b3b71bf910 |
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| 出典メモ | uspto-grants-2006_12 |
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