HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → Butyl-a-bromoacrylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Propanoic acid, 2,3-dibromo-, butyl ester | HCID 519844 | — |
| Catalyst | 4-Methoxyphenol | HCID 9015 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Butyl-a-bromoacrylate | HCID 19901948 | 90.9% |
Reaction Steps
The product (300 g) of Step 1 and p-methoxyphenol (2 g) was added to a 2 l. round bottom flask fitted with a thermometer, condenser, stirrer and inlet for nitrogen, and containing acetonitrile (1000 ml) and anhydrous potassium carbonate (330 g). The reaction mixture was stirred under reflux for 8 hours and cooled, and the salts were filtered off. The filtrate was evaporated under reduced pressure to remove the solvent, and the residue was dissolved in dichloromethane. The solution was dried (Na2SO4), filtered and evaporated. Distillation of the residue afforded n-butyl 2-bromoacrylate (196 g; 90%), b.p. 90°/15 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04414391 |
| Source dataset | uspto-grants-1983_11 |
| ORD ID | ord-1b01719e826d4861abd8b95da613c813 |
| Source note | uspto-grants-1983_11 |