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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585564Generated: October 27, 2026

Tetrahydrofuran → Tert-butyl (5-oxotetrahydrofuran-3-yl)acetate

https://huagongshe.com/reaction/585564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant2(5H)-FuranoneHCID 10341—
Reactanttert-Butyl acetateHCID 10908—
ReactantLithium diisopropylamide mono(tetrahydrofuran)HCID 10997623—
SolventWaterHCID 962—
ProductTert-butyl (5-oxotetrahydrofuran-3-yl)acetateHCID 1364187472%

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06933304B2
Source datasetuspto-grants-2005_08
ORD IDord-fc08a066caf44aa091c8db1dae39c476
Source noteuspto-grants-2005_08