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HRID 59690作成日:2026年10月25日
(R)-beta-aminophenethyl alcohol → (5)-N-((R)-2-hydroxy-1-phenylethyl)-2-methyl-5-phenylpentanamide
https://huagongshe.com/reaction/59690
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | (R)-beta-aminophenethyl alcohol | HCID 2724025 | — |
| 反応物 | HCID 90026070 | HCID 90026070 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (5)-N-((R)-2-hydroxy-1-phenylethyl)-2-methyl-5-phenylpentanamide | HCID 90025824 | 34% |
反応手順
To a solution consisting of (±)-2,5-dioxopyrrolidin-1-yl 2-methyl-5-phenyl pentanoate (18mb(i), 85.6 g, 296 mmol) in THF (3000 mL) at 48° C. was added R-(−)-2-phenylglycinol (65.9 g, 480 mmol, Bridge Organics) in portions. The resulting reaction mixture was stirred at 48° C. for 40 hours. A white precipitate formed, which was filtered from the reaction mixture and washed with THF. The filtrate was concentrated under vacuum and the residue, comprising the diastereomeric pair, was chromatographed on silica gel. Elution with ethyl acetate-heptane (50:50 v/v) afforded the pure diastereomer title compound (31.3 g, 34%) as a colorless solid; TLC Rf 0.205 (solvent system: 50:50 v/v ethyl acetate-heptane); HPLC retention time 15.1 minutes, stationary phase: Gemini 5μ C18 250×4.6 mm, ultraviolet detector at 210 nm, mobile phase: 1 mL/min, 60:40:0.1 v/v methanol-water-acetic acid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09440919B2 |
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| 出典データセット | uspto-grants-2016_09 |
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| ORD ID | ord-845b5e6a71054bcaa8d4933eb583801c |
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| 出典メモ | uspto-grants-2016_09 |
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