HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243530Generated: October 26, 2026
Tetrahydrofuran → Tert-butyl (5-oxotetrahydrofuran-3-yl)acetate
https://huagongshe.com/reaction/1243530
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2(5H)-Furanone | HCID 10341 | — |
| Reactant | tert-Butyl acetate | HCID 10908 | — |
| Reactant | Lithium diisopropylamide mono(tetrahydrofuran) | HCID 10997623 | — |
| Solvent | Water | HCID 962 | — |
| Product | Tert-butyl (5-oxotetrahydrofuran-3-yl)acetate | HCID 13641874 | 72% |
Reaction Steps
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)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07119098B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-46d7d26c0f8a4b6b8115e6491ccf613e |
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| Source note | uspto-grants-2006_10 |
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