HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → [Benzyl-(1-methyl-3-oxo-indan-5-yl)-amino]-acetic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Acetoxy-2-bromoethane | HCID 13564 | — |
| Reactant | N-(1-methyl-3-oxo-indan-5-yl)benzamide | HCID 86703337 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | [Benzyl-(1-methyl-3-oxo-indan-5-yl)-amino]-acetic acid ethyl ester | HCID 86703338 | 64.1% |
Reaction Steps
As presented in the following reaction formula, a solution of bromoethyl acetate (BrCH2COOEt; 7.5 g, 0.045 mol) in acetonitrile (20 mL) was added to a mixture of N-(1-methyl-3-oxo-indan-5-yl)benzamide (10 g, 0.037 mol) and anhydrous potassium carbonate (10.4 g, 0.075 mol) in acetonitrile (150 mL), and the reaction mixture was refluxed for 5 hours. After the completion of reaction, the mixture was filtered and the filtrate was concentrated to give the crude product [benzyl-(1-methyl-3-oxo-indan-5-yl)-amino]-acetic acid ethyl ester (8 g, yield: 63%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09242928B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-435b4880c8364418976bbac5ec0ddbed |
| Source note | uspto-grants-2016_01 |