関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | tert-butyl N-(4-oxocyclohexyl)carbamate | HCID 1512535 | — |
| 反応物 | Potassium tert-butoxide | HCID 23665647 | — |
| 触媒 | Butyltriphenylphosphonium bromide | HCID 159628 | — |
| 生成物 | HCID 86629083 | HCID 86629083 | — |
反応手順
To a mixture of potassium t-butoxide (2.05 g) and anhydrous N,N-dimethylformamide (60 ml) was added butyltriphenylphosphonium bromide (7.30 g) at room temperature. The mixture was stirred for 15 minutes and then a solution of t-butyl 4-oxocyclohexylcarbamate (1.30 g) in N,N-dimethylformamide (10 ml) was added to the mixture. The reaction mixture was stirred at room temperature overnight and then saturated aqueous ammonium chloride was added to the mixture. The mixture was extracted with toluene, and the organic layer was washed with brine, dried over sodium sulfate, and then the solvent was removed in vacuo. After diethyl ether was added to the residue, the precipitate was filtered off and then the filtrate was concentrated under reduced pressure. The residue was purified by a silica gel chromatography (eluent: gradient from 100% hexane/0% ethyl acetate to 0% hexane/100% ethyl acetate) to give 1.40 g of t-butyl (4-butylidenecyclohexyl)carbamate.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07767854B2 |
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| 出典データセット | uspto-grants-2010_08 |
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| ORD ID | ord-1fa0f1a583cb4d2886f66a95cb1ac0bd |
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| 出典メモ | uspto-grants-2010_08 |
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