関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | D-Glucose | HCID 5793 | — |
| 反応物 | 1-(4-(2-Methylpropyl)phenyl)-1-propanone | HCID 108834 | — |
| 反応物 | Ethanimidic acid, methyl ester, hydrochloride (1:1) | HCID 10313100 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | p-Isobutylpropiophenone dimethyl ketal | HCID 13298986 | — |
反応手順
To 11.33 g. (0.10 mole) of methyl acetimidate hydrochloride, prepared by known procedures, in a 100 ml. 3-necked, round-bottomed flask there was added a solution of 9.71 g. (actual 9.42 g.; 49.6 mmole) of crude p-isobutylpropiophenone, prepared as described in Part A above, in 23 ml. of absolute methanol. The resulting solution was stirred for 12 hours at room temperature to insure complete reaction. Gas liquid chromatographic analysis (Glc analysis) of an aliquot of the reaction mixture indicated greater than 99% ketal formation. The resulting mixture was filtered to remove the precipitated ammonium chloride and concentrated under vacuum. Hexane (50 ml.) was added to the residue and the resulting solution was again filtered to remove any acetamide which might be present. Removal of the hexane solvent under vacuum gave p-isobutylpropiophenone dimethyl ketal as a pale yellow oil which was used without further purification. The NMR was in accord.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04226790 |
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| 出典データセット | uspto-grants-1980_10 |
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| ORD ID | ord-675b331c6e4642918b98d571314f21c0 |
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| 出典メモ | uspto-grants-1980_10 |
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