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HRID 249432作成日:2026年10月26日
Diphenylacetaldehyde → (R)-1-(2-((2,2-Diphenylethenyl)oxy)ethyl)-3-piperidinecarboxylic acid ethyl ester
https://huagongshe.com/reaction/249432
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Diphenylacetaldehyde | HCID 13696 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | (R)-1-(2-bromoethyl)nipecotic acid ethyl ester hydrobromide | HCID 70009171 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | (R)-1-(2-((2,2-Diphenylethenyl)oxy)ethyl)-3-piperidinecarboxylic acid ethyl ester | HCID 10621814 | 69.6% |
反応手順
Diphenylacetaldehyde (4.9 g, 0.025 mole) was added dropwise to a mixture of sodium hydride (1.5 g, 0.05 mole, 80% oil dispersion) and dry toluene (25 ml) at 0° C. This mixture was stirred at room temperature for 0.5 h, heated to 50° C. and allowed to cool to room temperature. The above (R)-1-(2-bromoethyl)nipecotic acid ethyl ester hydrobromide (8.6 g, 0.025 mole) was added portionwise whilst the temperature was kept below 30° C. with an ice-water bath. After being stirred for 1 h the reaction mixture was filtered, and the filtrate was evaporated to dryness. Flash chromatography of the residue on silica gel (200 g) using a mixture of heptane and tetrahydrofuran (4/1) as eluent provided the title compound (6.6 g, 69%) as an oil. Tlc: rf 0.24 (SiO2 ; heptane/THF 7/3).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05214057 |
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| 出典データセット | uspto-grants-1993_05 |
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| ORD ID | ord-6008a16e2291462b970111ccd9e58c04 |
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| 出典メモ | uspto-grants-1993_05 |
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