関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 5-Hexenal | HCID 69817 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | (R)-1-(4-isopropyl-2-thioxothiazolidin-3-yl)ethanone | HCID 11745744 | — |
| 触媒 | Titanium Tetrachloride | HCID 24193 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | (R)-3-Hydroxy-1-((R)-4-isopropyl-2-thioxothiazolidin-3-yl)oct-7-en-1-one | HCID 59644064 | 74% |
反応手順
A solution of (R)-1-(4-isopropyl-2-thioxothiazolidin-3-yl)ethanone (11.8 g, 58.1 mmol) in dichloromethane (380 mL) under an atmosphere of nitrogen was cooled to −78° C., titanium tetrachloride (6.37 mL, 58.1 mmol) was added, and the mixture was stirred for 10 min. Diisopropylethylamine (10.12 mL, 58.1 mmol) was added, and the mixture was stirred for 1 h at −78° C. A 1 M solution of hex-5-enal (58.1 mL, 58.1 mmol) in dichloromethane was added, and the mixture was stirred for 2 h at −78° C. The reaction was quenched by addition of half-saturated NH4Cl (30 mL) and warmed to room temperature. The mixture was extracted twice with dichloromethane, and the organic phase was dried and evaporated to provide a residue. Chromatography on silica gel afforded the title compound (12.92 g, 74%). This procedure has also been carried out using the (R)-1-(4-benzyl-2-thioxothiazolidin-3-yl)ethanone auxiliary, with a similar result.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07320974B2 |
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| 出典データセット | uspto-grants-2008_01 |
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| ORD ID | ord-538157f1bdb54ee8ada57adc71242da2 |
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| 出典メモ | uspto-grants-2008_01 |
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