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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371106Generated: October 31, 2026

Benzyl Aziridine-1-carboxylate → HCID 69246152, compound

https://huagongshe.com/reaction/2371106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl Aziridine-1-carboxylateHCID 9855625—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantTert-butyl 5-biphenyl-4-yl-3-oxopentanoateHCID 58914664—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69246152HCID 6924615216.4%

Reaction Steps

To a solution of the compound tert-butyl 5-biphenyl-4-yl-3-oxopentanoate (237 mg,) in tetrahydrofuran (4 ml) and tert-butyl alcohol (4 ml) at 0° C. under inert atmosphere was added potassium tert-butoxide (98 mg) and stirred for 20 minutes. To this at 0° C. was then added n-tetrabutylammonium iodide (27 mg) and benzyl aziridine-1-carboxylate (130 mg) and stirred the reaction mixture for 5 minutes. The resulting reaction mixture was warmed to room temperature and then further heated at 70° C. for 2 hours. The solvent was evaporated under reduced pressure and the residue thus obtained was taken in water and extracted with ethyl acetate. The combined organic layers were washed with water and brine, dried over anhydrous sodium sulphate and concentrated under reduced pressure. The residue thus obtained was purified by column chromatography using 20% ethyl acetate in hexane as eluant to furnish the title compound (60 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710261B2
Source datasetuspto-grants-2014_04
ORD IDord-210cc8daabfe4ceb80983698db88bd1f
Source noteuspto-grants-2014_04