HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Chloroperbenzoic acid → 3-Aminobicyclo[1.1.1]pentan-1-yl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 1-{3-Aminobicyclo[1.1.1]pentan-1-yl}ethan-1-one | HCID 90410811 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-Aminobicyclo[1.1.1]pentan-1-yl acetate | HCID 90411187 | — |
Reaction Steps
A solution of 1-(3-aminobicyclo[1.1.1]pentan-1-yl)ethanone (1 mmol) in 0.5 mL of chloroform is added to a stirred mixture of m-chloroperbenzoic acid (1.5 mmol) in 2 mL of chloroform at room temperature. The solution is stirred in the dark for 24 h. The mixture is filtered, and the filtrate is washed with 10% sodium bicarbonate and then water. The organic layer is dried over magnesium sulfate and concentrated. The residue is purified by a flash chromatography on silica gel (EtOAc/hexnaes) to give 3-aminobicyclo[1.1.1]pentan-1-yl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09447025B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-fb450d3fc7074525b2fcf30ca36b5bee |
| Source note | uspto-grants-2016_09 |