HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-[(1E)-3-ethoxy-3-oxoprop-1-en-1-yl]benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | 3-Iodobenzoic acid | HCID 12060 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-[(1E)-3-ethoxy-3-oxoprop-1-en-1-yl]benzoic acid | HCID 10489084 | 104.3% |
Reaction Steps
A solution of 3-iodobenzoic acid (20.2 g, 81.4 mmol), ethyl acrylate (9.0 g, 90.2 mmol), triethylamine (24 mL) and palladium acetate (92 mg, 0.41 mmol) in DMF (130 mL) was stirred at 140° C. for 3 hr. The reaction mixture was cooled to room temperature, partitioned between ethyl acetate and 1N hydrochloric acid, and the ethyl acetate layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure and the obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate 50:50-0:100) to give the title compound (18.7 g, quant.) as an orange solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08586571B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-c6e8a7db4a024229ae59b78527dc5c8b |
| Source note | uspto-grants-2013_11 |