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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1931536Generated: November 4, 2026

2-Ethyl-1-butene → HCID 58432618, compound

https://huagongshe.com/reaction/1931536

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Ethyl-1-buteneHCID 12970—
ReactantTosylchloramideHCID 31388—
ReactantPhenyltrimethylammonium bromide dibromideHCID 17977687—
SolventAcetonitrileHCID 6342—
ProductHCID 58432618HCID 5843261840.5%

Reaction Steps

Chloramine-T (10 g, 43.9 mmol) was suspended in acetonitrile (146 mL) at room temperature under nitrogen. To this suspension was added 2-ethylbut-1-ene (5.55 g, 65.9 mmol) followed by phenyltrimethylammonium tribromide (1.65 g, 4.39 mmol) in two roughly equal portions. After three days the reaction mixture was concentrated to half volume and then filtered through a sintered glass funnel. The filtrate was concentrated to half volume again which caused further precipitation. This mixture was filtered and the filtrate was partitioned between ethyl acetate and water. The organic phase was dried with MgSO4, filtered and concentrated. The crude material was purified by column chromatography using a Biotage 65i column eluting with (0-100% EtOAc/hexane) to give 2,2-diethyl-1-[(4-methylphenyl)sulfonyl]-aziridine as a colorless solid (4.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188085B2
Source datasetuspto-grants-2012_05
ORD IDord-b9ff39559fa84644bb8b81da23cef529
Source noteuspto-grants-2012_05