関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methanol | HCID 887 | — |
| 反応物 | Quinoline | HCID 7047 | — |
| 反応物 | N-(3-Butylphenyl)-3-oxobutanamide | HCID 21445129 | — |
| 反応物 | Methylorthoformate | HCID 53629101 | — |
| 触媒 | p-Toluenesulfonic acid | HCID 6101 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | m-(n-Butyl)-3-methoxy-crotonanilide | HCID 70633214 | 69.9% |
反応手順
A mixture of 8.5 g of m-(n-butyl)-acetylacetanilide, 5.7 g of methyl orthoformate, 80 ml of methanol and 0.3 g of p-toluene sulfonic acid was stirred at 20° C for 16 hours and after the addition of 100 ml of toluene and 0.6 ml of quinoline, the mixture was heated at 140° C for one hour while distilling the toluene-methanol azeotrope. After refluxing for 30 minutes, another 100 ml of toluene were added thereto and the reaction was completed when the solvent was evaporated. The residue was chromatographed over silica gel and elution with an 8-2 mixture of methylene chloride and ethyl acetate yielded 6.3 g of m-(n-butyl)-3-methoxy-crotonanilide melting at 36° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04014679 |
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| 出典データセット | uspto-grants-1977_03 |
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| ORD ID | ord-f51aa030a367463d964046e727788549 |
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| 出典メモ | uspto-grants-1977_03 |
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