関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | 2(5H)-Furanone | HCID 10341 | — |
| 反応物 | tert-Butyl acetate | HCID 10908 | — |
| 反応物 | Lithium diisopropylamide mono(tetrahydrofuran) | HCID 10997623 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | Tert-butyl (5-oxotetrahydrofuran-3-yl)acetate | HCID 13641874 | 72% |
反応手順
Tetrahydrofuran (50 mL) and Lithium diisopropylamide mono tetrahydrofuran complex (20 mL of 1.5 M in cyclohexane) was cooled in a dry ice/Isopropanol bath for 10 min. Tert-butyl acetate (3.5 mL 26 mmoles) was added via syringe and stirred at −78° C. for 30 min. 2(5H)-Furanone (1.59 g, 19 mmoles) was added dropwise and the reaction was stirred for 1 h at −78° C. The reaction was poured into water and extracted with ether 2×150 mL The ether extracts were combined and washed with water 100 mL then brine 3×100 mL, dried and the ether removed under reduced pressure to give 2.74 g of product (72%). MS (ESI+) for C10H16O4 m/z 223 (M+Na)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06933304B2 |
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| 出典データセット | uspto-grants-2005_08 |
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| ORD ID | ord-fc08a066caf44aa091c8db1dae39c476 |
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| 出典メモ | uspto-grants-2005_08 |
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