Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2355436Generated: October 26, 2026

1-Allyl-1-cyclohexanol → 1-((1-Tosylaziridin-2-yl)methyl)cyclohexanol

https://huagongshe.com/reaction/2355436

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Allyl-1-cyclohexanolHCID 79145—
ReactantN-tosyliminophenyliodinaneHCID 86611515—
Catalystcopper(II) trifluoromethanesulfonateHCID 2734996—
SolventAcetonitrileHCID 6342—
Product1-((1-Tosylaziridin-2-yl)methyl)cyclohexanolHCID 5938283113.3%

Reaction Steps

A flame-dried 100 mL three-necked flask was purged with N2, and charged with Cu(OTf)2 (95 mg, 0.26 mmol), 1-allylcyclohexanol (960 mg, 9.86 mmol) and acetonitrile (HPLC grade). Solid [N-(p-Toluenesulfonyl)imino]phenyliodinane (PhINTs, prepared as described in Inorgania Chimica Acta 2003, 342, 301-304, 1.97 g, 5.28 mmol) was added in a single portion and the mixture was stirred at rt until all PhINTs had dissolved (within 5 to 30 min). The solvent was removed and the residue was chromatographied on silica gel eluted with hexane/EtOAc to give 1-((1-tosylaziridin-2-yl)methyl)cyclohexanol (217 mg, 13%). MS m/z 310 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754737B2
Source datasetuspto-grants-2010_07
ORD IDord-f89b4bc76fcb4badac74c5596ef86fce
Source noteuspto-grants-2010_07