関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1,3-Dimethyl-2-imidazolidinone | HCID 6661 | — |
| 反応物 | Allyl chloride | HCID 7850 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| 反応物 | 3-Hydroxybutyrolactone, (3S)- | HCID 7269389 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (2S,3S)-2-allyl-3-hydroxy-gamma-butyrolactone | HCID 20675472 | 75% |
反応手順
Lithium hexamethyldisilazide (5.1 ml, 5.1 mmol) was loaded under argon gas in a reaction vessel. (S)-3-Hydroxy-γ-butyrolactone (0.250 g, 2.449 mmol) in THF (5 ml) was added thereto under cooling to −45° C. After stirring for 30 minutes at the same temperature, allyl chloride (0.24 ml, 2,94 mmol) and 1,3-dimethyl-2-imidazolidinone (0.7 ml) in THF (5 ml) was dropped thereto. After stirring for 30 minutes at the same temperature, an aqueous saturated ammonium chloride was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over magnesium sulfate, and condensed in vacuo. The residue was purified by silica gel chromatography to give (2S,3S)-2-allyl-3-hydroxy-γ-butyrolactone (0.261 g, yield 75%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06268515B1 |
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| 出典データセット | uspto-grants-2001_07 |
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| ORD ID | ord-bbbe6aecca904c5398a997f0604282ad |
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| 出典メモ | uspto-grants-2001_07 |
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