HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 3-(3-bromophenyl)acrylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | m-Bromocinnamic acid | HCID 776461 | — |
| Product | Ethyl 3-(3-bromophenyl)acrylate | HCID 5369361 | — |
Reaction Steps
Trans m-bromocinnamic acid (14.8 g), ethanol (173 ml) and concentrated sulfuric acid (0.4 ml) were combined and heated at reflux for 15 hours. About 150 ml of the ethanol was distilled off, and the remaining solution was poured into ice/water (140 ml). The cold mixture was made strongly alkaline with 40% sodium hydroxide and extracted with methylene chloride (4 × 60 ml). The combined methylene chloride extract was dried over anhydrous potassium carbonate. The potassium carbonate was removed by filtration and the solvent stripped off under reduced pressure. Trans ethyl 3-bromocinnamate, was obtained as a partially solidified oil. (IR spectrum was consistent with this compound).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04091112 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-9870d426fd5b4195b7ebc741da7d9143 |
| Source note | uspto-grants-1978_05 |