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HRID 16602作成日:2026年10月27日
Benzyl Alcohol → tert-Butyl [{1-(2-benzyloxycarbonyl-2-methylpropyl)piperidin-4-yl}methyl]carbamate
https://huagongshe.com/reaction/16602
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Benzyl Alcohol | HCID 244 | — |
| 反応物 | Sodium Iodide | HCID 5238 | — |
| 反応物 | 3-Chloro-2,2-dimethylpropanoyl chloride | HCID 61345 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | Tert-butyl (piperidin-4-ylmethyl)carbamate | HCID 723429 | — |
| 反応物 | Benzyl 3-chloropivalate | HCID 54294282 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | tert-Butyl [{1-(2-benzyloxycarbonyl-2-methylpropyl)piperidin-4-yl}methyl]carbamate | HCID 86602121 | 1.3% |
反応手順
To a stirred solution of tert-butyl (piperidin-4-ylmethyl)carbamate (38.8 g, 181 mmol) in N,N-dimethylformamide (100 mL) was added benzyl 3-chloropivalate {14.2 g, 124 mmol, prepared from 3-chloropivaloyl chloride (25.6 g, 165 mmol) and benzyl alcohol (19.6 g, 181 mmol), ethyldiisopropylamine (64.0 g, 495 mmol) and sodium iodide (27.1 g, 181 mmol) at ambient temperature. The resulting mixture was stirred at 120° C. for 14 h. The volatile components were removed by evaporation and the resulting residue was chromatographed on a column of silica gel eluting with hexane/ethyl acetate (1:1) to give 640 mg (1%) of the title compound as a pale yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07737163B2 |
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| 出典データセット | uspto-grants-2010_06 |
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| ORD ID | ord-51017605c27a4df0905c4c42548db89d |
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| 出典メモ | uspto-grants-2010_06 |
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