関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Arecoline | HCID 2230 | — |
| 反応物 | HCID 178418676 | HCID 178418676 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | Methyl 4-(4-fluorophenyl)-1-methylpiperidine-3-carboxylate | HCID 9794957 | — |
反応手順
A 2 molar solution of 4-fluorophenylmagnesium bromide in diethyl ether (5 ml, 2 molar equivalents) was stirred at −5 to −10° C. under nitrogen, and a solution of arecoline (0.78 g) in toluene (5.0 ml) added over 15 minutes at −5° C. The clear solution was stirred at −5° C. for 1 hour, then quenched by the addition of a mixture of water (25 ml) and concentrated hydrochloric acid (3 ml). Analysis of the aqueous phase by HPLC showed that yield of cis/trans 1-methyl-3-carbomethoxy-4-(4-fluorophenyl)-piperidine was about 905 mg (72 %).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06172233B2 |
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| 出典データセット | uspto-grants-2001_01 |
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| ORD ID | ord-66bf9d8dd4b54bdcba0f55494e40c544 |
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| 出典メモ | uspto-grants-2001_01 |
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