HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Chloroperbenzoic acid → Acetic acid 4-benzyloxy-2-((R)-1-oxiranylmethoxy)phenyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-[4-Benzyloxy-2-((R)-1-oxiranylmethoxy)phenyl]ethanone | HCID 86644713 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Acetic acid 4-benzyloxy-2-((R)-1-oxiranylmethoxy)phenyl ester | HCID 86644714 | — |
Reaction Steps
To a stirred solution of 1-[4-benzyloxy-2-((R)-1-oxiranylmethoxy)phenyl]ethanone (1.62 g, 5.43 mmol) in DCM (60 ml) was added m-chloroperbenzoic acid (2.15 g) and solid NaHCO3 (3.24 g). Stirring was continued at 40° C. for 1 h. The mixture was filtered and the filtrate was washed once with 10% NaHSO4 solution and then twice with NaHCO3 solution. The organic layer was washed with water and brine, dried with Na2SO4. The solvent was removed under reduced pressure. The crude product obtained (1.34 g) was sufficiently pure for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08809536B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-4575784bd80049e791f527d5c050003f |
| Source note | uspto-grants-2014_08 |