関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1-Bromo-3-chloropropane | HCID 8006 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 1,2,3,6-Tetrahydro-4-phenylpyridine | HCID 82553 | — |
| 反応物 | 1-(3-Chloropropyl)-4-phenylpiperidine | HCID 203689 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 1-(3-Chloropropyl)-4-phenyl-1,2,3,6-tetrahydropyridine | HCID 9837583 | — |
反応手順
1-(3-Chloropropyl)-4-phenyl-1,2,4,6-tetrahydropyridine can be prepared as follows: a solution of 1-bromo-3-chloropropane (6 cc) and 4-phenyl-1,2,3,6-tetrahydropyridine (5.1 g) in acetonitrile (60 cc) is stirred at 25° C. for 20 hours with potassium carbonate (97 g). The mixture is filtered and then concentrated to dryness under reduced pressure (2.7 kPa). The residue is chromatographed on a column of silica gel (0.2-0.063-mm particle size, 4-cm diameter, 40-cm height) and eluted with a mixture of cyclohexane and ethyl acetate (50--50 by volume), 250-cc fractions being collected. Fractions 7 to 13 are combined and concentrated to dryness under reduced pressure (2.7 kPa) to give 1-(3-chloropropyl)-4-phenyl-1,2,3,6-tetrahydropyridine (5 g) in the form of a yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05130313 |
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| 出典データセット | uspto-grants-1992_07 |
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| ORD ID | ord-b29375861d594433a16ffd83ce2d1d0a |
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| 出典メモ | uspto-grants-1992_07 |
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