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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921917Generated: November 1, 2026

Aziridine → Benzyl Aziridine-1-carboxylate

https://huagongshe.com/reaction/1921917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAziridineHCID 9033—
ReactantBenzyl chloroformateHCID 10387—
ReactantPotassium CarbonateHCID 11430—
SolventDiethyl EtherHCID 3283—
ProductBenzyl Aziridine-1-carboxylateHCID 9855625—

Reaction Steps

To a stirred, distilled aziridine solution (500 m, 0.1 mol) in a round-bottom flask cooling with an ice bath, three equivalents of potassium carbonate was added. After all of the solid dissolved, benzyl chloroformate (1.5 equivalents) in ethyl ether (150 mL) was added over 2 h. The solution was stirred overnight and warmed to room temperature, and the aqueous phase was extracted with methylene chloride (5×30 mL). The organic phases were combined and passed through a flash silica gel pad and concentrated to afford the Cbz-aziridine as colorless thick oil, yield: 7.2 g, 81%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173800B2
Source datasetuspto-grants-2012_05
ORD IDord-a193886b52214428865337961667acc5
Source noteuspto-grants-2012_05