HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propanal → Ethyl 3-chloro-2-oxopentanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propanal | HCID 527 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Ethyl dichloroacetate | HCID 10808 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Product | Ethyl 3-chloro-2-oxopentanoate | HCID 13719444 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
Sodium ethoxide (0.68 g, 9.94 mmol) was added portionwise to a mixture of ethyldichloroacetate (1.22 ml, 9.94 mmol) and diethyl ether (10 ml) under ice-water cooling and the resulting mixture was stirred at 0° C. for 30 minutes. Propionaldehyde (0.79 ml, 10.93 mmol) was then added and the reaction mixture allowed to warm to room temperature slowly and stirring continued for 72 hours. The reaction mixture was then poured onto water (10 ml) and extracted with diethyl ether (2×15 ml). The organic layers were combined, dried over magnesium sulfate, and concentrated in vacuo to yield crude 3-chloro-2-oxo-pentanoic acid ethyl ester (1.8 g) which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07700634B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-5308c45182cf4ab583db80ba46a4ea2d |
| Source note | uspto-grants-2010_04 |