HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → 1-[3-(Ethoxycarbonylmethoxy)benzoyl]-2-(4,5-diphenyl-2-oxazolyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(3-Hydroxybenzoyl)-2-(4,5-diphenyl-2-oxazolyl)piperidine | HCID 18367315 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-[3-(Ethoxycarbonylmethoxy)benzoyl]-2-(4,5-diphenyl-2-oxazolyl)piperidine | HCID 18367244 | 74.8% |
Reaction Steps
A mixture of 1-(3-hydroxybenzoyl)-2-(4,5-diphenyl-2-oxazolyl)piperidine (100 mg), ethyl bromoacetate (61 mg), and K2CO3 (84 mg) in acetonitrile (1.0 ml) was stirred at room temperature overnight and partitioned between water and ethyl acetate. The organic layer was separated, washed with water and brine, dried over MgSO4, and evaporated in vacuo. The residue was chromatographed over silica gel to afford 1-[3-(ethoxycarbonylmethoxy)benzoyl]-2-(4,5-diphenyl-2-oxazolyl)piperidine (90 mg) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05972965 |
| Source dataset | uspto-grants-1999_10 |
| ORD ID | ord-5130e6490eba410d84bb5605b211fdd7 |
| Source note | uspto-grants-1999_10 |