HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl formate → Ethyl 2-(benzyloxy)-3-oxopropanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl formate | HCID 8025 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 2-(benzyloxy)acetate | HCID 290299 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Ethyl 2-(benzyloxy)-3-oxopropanoate | HCID 19903223 | — |
Reaction Steps
To a suspension of sodium hydride (3.3 g, 60% in paraffin oil, 82.5 mmol) in dry ether (100 mL) and dry ethyl formate (5.55 g, 75 mmol) was added ethyl (benzyloxy)acetate (14.57 g, 75 mmol) dropwise with stirring. The resulting mixture solution was then refluxed for 2 h and concentrated to give crude ethyl 2-(benzyloxy)-3-oxopropanoate which was used in the subsequent step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08969364B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-bf3ba2740770454b819b381849387ac0 |
| Source note | uspto-grants-2015_03 |