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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Aziridine-1-carboxylate | HCID 9855625 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | Tert-butyl 5-biphenyl-4-yl-3-oxopentanoate | HCID 58914664 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69246152 | HCID 69246152 | 16.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08710261B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-210cc8daabfe4ceb80983698db88bd1f |
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| Source note | uspto-grants-2014_04 |
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