関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| 反応物 | 1-(2,2,4-Trimethyl-3-cyclohexen-1-yl)ethan-1-one | HCID 3016988 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 1-(2,2,4-trimethyl-cyclohex-3-enyl)-ethanone O-methyl-oxime | HCID 86675338 | 92.4% |
反応手順
To a stirred solution of 1-(2,2,4-trimethyl-cyclohex-3-enyl)-ethanone (162 g; 0.97 mol), prepared as described in example P4, in methanol (500 ml) was added pyridine (160 ml; 1.95 mol) followed by a portionwise addition of methoxyamine hydrochloride (142 g; 1.70 mol). The reaction mixture was stirred at 24° C. for 16 hours under nitrogen atmosphere. Methanol was removed under reduced pressure, the residue poured in water (600 ml) and 1N hydrochloric acid was added (100 ml). The solution was extracted with dichloromethane (3×300 ml). Combined organic layers were washed with brine (500 ml) and dried over sodium sulfate. The solvent was removed in vacuo to afford 175 g (92% of theory) of 1-(2,2,4-trimethyl-cyclohex-3-enyl)-ethanone O-methyl-oxime as a clear red oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08536215B2 |
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| 出典データセット | uspto-grants-2013_09 |
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| ORD ID | ord-949bef1b62f54a69bbcb37a365ea0c46 |
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| 出典メモ | uspto-grants-2013_09 |
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