HuagongsheHuagongshe Chemistry Print Report · For research reference only
Beta-Propiolactone → HCID 20135581, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Beta-Propiolactone | HCID 2365 | — |
| Reactant | 2,3-Dichloro-4-hydroxybenzaldehyde | HCID 528380 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 20135581 | HCID 20135581 | — |
Reaction Steps
2,3-dichloro-4-hydroxybenzaldehyde (38.2 g., 0.2 mole) is dissolved in a 10% sodium hydroxide solution (200 ml.). The solution is heated to boiling and β-propiolactone (144 g., 2.0 moles) is added dropwise at such a rate as to keep the solution boiling. During the addition 10% sodium hydroxide solution is added in portions to maintain an alkaline mixture. Then the solution is cooled and acidified. The precipitated material is dissolved in ether and the product is extracted into a 5% sodium bicarbonate solution. Acidification of the aqueous solution precipitates 3-(2,3-dichloro-4-formylphenoxy)propionic acid, which is purified by recrystallization from ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04751244 |
| Source dataset | uspto-grants-1988_06 |
| ORD ID | ord-34c4669876e5496c9e800ddd0ff089ff |
| Source note | uspto-grants-1988_06 |