참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | 2(5H)-Furanone | HCID 10341 | — |
| 반응물 | tert-Butyl acetate | HCID 10908 | — |
| 반응물 | Lithium diisopropylamide mono(tetrahydrofuran) | HCID 10997623 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | Tert-butyl (5-oxotetrahydrofuran-3-yl)acetate | HCID 13641874 | 72% |
반응 단계
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)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06933304B2 |
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| 출처 데이터셋 | uspto-grants-2005_08 |
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| ORD ID | ord-fc08a066caf44aa091c8db1dae39c476 |
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| 출처 메모 | uspto-grants-2005_08 |
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