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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577740Generated: October 30, 2026

Ethyl Acetate → HCID 178454125, compound

https://huagongshe.com/reaction/577740

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantLithiumHCID 3028194—
Reactanttert-Butyl 3-oxocyclobutylcarbamateHCID 23374584—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178454125HCID 178454125613.2%

Reaction Steps

To a solution of tert-butyl (3-oxocyclobutyl)carbamate (100 g, 54 mmol) in THF (2000 mL) at −72° C. was added dropwise a solution of lithium trisec-butylhidridoborate (648 mL, 1 M) in THF over 1.5 hrs. The resulting solution was allowed to warm up to rt and stirred for another 1 hr. TLC (petroleum ether: EtOAc=2:1) showed that the starting material was consumed completely. The reaction was quenched with NH4Cl aqueous. Water (1000 mL) and EtOAc (2000 mL) were added to the mixture. The organic layer was separated, dried over MgSO4 and concentrated to give crude material, which was purified by column chromatography with petroleum ether: EtOAc from 10:1 to 1:2 to afford the title compound (62 g, 61% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040547B2
Source datasetuspto-grants-2015_05
ORD IDord-e2636a274d834bffa6e30f06fe521511
Source noteuspto-grants-2015_05