HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Chloroperbenzoic acid → HCID 21936588, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 21936603 | HCID 21936603 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 21936588 | HCID 21936588 | 100% |
Reaction Steps
A solution of tert-butyl 2-[2-(2-methyl-1H-imidazo[4,5-c]quinolin-1-yl)ethoxy]ethylcarbamate (10.75 g, 29.0 mmol) in 150 mL of CHCl3 was chilled in an ice water bath. The solution was treated with 3-chloroperoxybenzoic acid (MCPBA, 70%, 10.73 g, 43.5 mmol). After stirring for 1.5 h, the reaction mixture was washed with 1% Na2CO3 (3×) solution and the layers were separated. The organic portion was washed with H2O and brine then dried over Na2SO4 and concentrated to give a sticky brown solid. The solid was triturated with ether to yield 11.21 g of tert-butyl 2-[2-(2-methyl-5-oxido-1H-imidazo[4,5-c]quinolin-1-yl)ethoxy]ethylcarbamate as a light tan solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06677347B2 |
| Source dataset | uspto-grants-2004_01 |
| ORD ID | ord-1523ffb2ce684178b04dddf2009bb64f |
| Source note | uspto-grants-2004_01 |