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HRID 458385作成日:2026年10月25日
2-Naphthalenesulfonyl chloride → 4-Hydroxy-1-(naphthalene-2-sulfonyl)-1,2,5,6-tetrahydro-pyridine-3-carboxylic acid ethyl ester
https://huagongshe.com/reaction/458385
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 2-Naphthalenesulfonyl chloride | HCID 7125 | — |
| 反応物 | 3-Piperidinecarboxylic acid, 4-oxo-, ethyl ester, hydrochloride (1:1) | HCID 107315 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Hexamethyldisilazane | HCID 13838 | — |
| 生成物 | 4-Hydroxy-1-(naphthalene-2-sulfonyl)-1,2,5,6-tetrahydro-pyridine-3-carboxylic acid ethyl ester | HCID 69432328 | 97.9% |
反応手順
A suspension of 31.15 g (150 mmol) 3-Ethoxycarbonyl-4-piperidone hydrochloride was suspended in 400 ml hexamethyldisilazane and heated under reflux (140° C.) for 2.5 h. The solution was evaporated complete, the residue dissolved in 400 ml THF and treated with 34 g (150 mmol) of naphthalene-2-sulfonylchloride in 150 ml THF. The reaction was stirred 16 h at room temperature, evaporated, treated with 400 ml aqueous 10% NaCl, stirred for 10 min and extracted with EtOAc (3×400 ml). The organic phase was dried (Na2SO4) and evaporated and crystallized from Et2O at 5° C. to give 53.1 g (90%) of 4-hydroxy-1-(naphthalene-2-sulfonyl)-1,2,5,6-tetrahydro-pyridine-3-carboxylic acid ethyl ester, MS: 362 (MH+).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07189756B2 |
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| 出典データセット | uspto-grants-2007_03 |
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| ORD ID | ord-5b798cdf8ee94f53ae60e11e60566366 |
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| 出典メモ | uspto-grants-2007_03 |
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