関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Diethyl Ether | HCID 3283 | — |
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | 4-(Dimethylamino)-4-phenylcyclohexan-1-one | HCID 11424492 | — |
| 触媒 | Butyltriphenylphosphonium bromide | HCID 159628 | — |
| 生成物 | (4-Butylidene-1-phenyl-cyclohexyl)-dimethylamine | HCID 68632980 | — |
反応手順
Potassium tert-butylate (2.75 g, 23.7 mmol) was provided in abs. ether (50 mL) in argon and mixed with butyl-triphenyl phosphonium bromide (9.45 g, 23.7 mmol). The batch was heated for 30 min to 40° C. 4-dimethylamino-4-phenyl cyclohexanone (5.00 g, 23.0 mmol) dissolved in abs. THF (50 mL) was then added carefully in drops (exothermic reaction). The batch was heated for 6.5 h to 50° C. and stirred overnight at room temperature. The batch was then concentrated in a vacuum until dry, taken up in dioxan (20 mL) and mixed with HCl/dioxan (5 mL). A precipitate separated out during this. This was filtered off, washed with ether (10 mL), then basified with 2N NaOH and extracted with dichloromethane (2×40 mL). The organic phase was dried over Na2SO4, filtered and concentrated in a vacuum until dry.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08835689B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-fe2b2fc9c85a469fbf94e00b697aa1df |
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| 出典メモ | uspto-grants-2014_09 |
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