関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Benzyl Bromide | HCID 7498 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 3-benzyloxy-4-hydroxy-5-(2-hydroxyethyl)-2(5H)-furanone | HCID 54723596 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 3,4-dibenzyloxy-5-(2-hydroxyethyl)-2(5H)-furanone | HCID 21184106 | 60% |
反応手順
A mixture of 1.25 g (5 mmol) of 3-benzyloxy-4-hydroxy-5-(2-hydroxyethyl)-2(5H)-furanone, 15 mL of THF, 871 μL (5.0 mmol) of diisopropylethylamine and 631 μL (5.2 mmol) of benzyl bromide were combined under argon. The reaction mixture was warmed to reflux for 5 hours, and upon cooling, a suspension formed which was poured into 50 mL of 5% aqueous HCl solution and extracted with 100 mL of ether. The ether fraction was separated and sequentially washed with 30 mL of 5% aqueous HCl, 30 mL of H2O, 30 mL of saturated NaHCO3 solution, 30 mL of H2O, 30 mL of brine, dried (MgSO4) and concentrated to a colorless oil. Purification over silica gel using EtOAc/hexanes (2/3) provided 3,4-dibenzyloxy-5-(2-hydroxyethyl)-2(5H)-furanone as a faint pink colored oil (1.0 g, 60% yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06262073B1 |
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| 出典データセット | uspto-grants-2001_07 |
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| ORD ID | ord-cb7ac1c9ba61482b871363cbb05890b1 |
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| 出典メモ | uspto-grants-2001_07 |
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