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HRID 380128作成日:2026年10月26日
2-Bromo-1,2-diphenylethan-1-one → 2-Oxo-1,2-diphenylethyl 1-(3-benzyloxybenzoyl)-2-piperidinecarboxylate
https://huagongshe.com/reaction/380128
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-Bromo-1,2-diphenylethan-1-one | HCID 102630 | — |
| 反応物 | Sodium | HCID 5360545 | — |
| 反応物 | 1-(3-Benzyloxybenzoyl)-2-piperidinecarboxylic acid | HCID 18367416 | — |
| 触媒 | Sulfuric Acid | HCID 1118 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 2-Oxo-1,2-diphenylethyl 1-(3-benzyloxybenzoyl)-2-piperidinecarboxylate | HCID 54247856 | 28.4% |
反応手順
Sodium (54 mg) was dissolved in ethanol (8.0 ml), and then 1-(3-benzyloxybenzoyl)-2-piperidinecarboxylic acid (665 mg), conc. sulfuric acid (1 drop), and desyl bromide (539 mg) was successively dissolved thereto. The resulting mixture was stirred at 70° C. for 2 days, cooled to room temperature, and partitioned between ethyl acetate and 1N HCl. The organic layer was washed with 1N HCl, aqueous sodium bicarbonate, and brine, dried over MgSO4, and evaporated in vacuo. The residue was chromatographed over silica gel to afford 2-oxo-1,2-diphenylethyl 1-(3-benzyloxybenzoyl)-2-piperidinecarboxylate (297 mg) 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 | US06300344B1 |
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| 出典データセット | uspto-grants-2001_10 |
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| ORD ID | ord-969536c747cd4b3a94fb701bec284060 |
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| 出典メモ | uspto-grants-2001_10 |
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