HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Allyl-1-cyclohexanol → 1-((1-Tosylaziridin-2-yl)methyl)cyclohexanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Allyl-1-cyclohexanol | HCID 79145 | — |
| Reactant | N-tosyliminophenyliodinane | HCID 86611515 | — |
| Catalyst | copper(II) trifluoromethanesulfonate | HCID 2734996 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-((1-Tosylaziridin-2-yl)methyl)cyclohexanol | HCID 59382831 | 13.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08455521B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-780333f8af1742eda1ffa10ba324d5d1 |
| Source note | uspto-grants-2013_06 |