HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336702Generated: October 25, 2026
Triethylamine → Ethyl 3-(4-formylphenyl)propanoate
https://huagongshe.com/reaction/336702
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3,3-Diethoxy-1-propene | HCID 62477 | — |
| Reactant | 4-Iodobenzaldehyde | HCID 96657 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 3-(4-formylphenyl)propanoate | HCID 12169276 | 711.8% |
Reaction Steps
To a solution of 4-iodobenzaldehyde (0.116 g, 0.5 mmol), acrolein diethylacetal (0.3 mL, 1.5 mmol), tetra-n-butylammonium chloride (0.139 g, 0.5 mmol) and triethylamine in anhydrous dimethylformamide (2 mL), palladium acetate (0.003 g, 0.015 mmol) was added. The reaction mixture was heated at 90° C. and stirred for 16 h. The reaction mixture was diluted with 2 N hydrochloric acid and extracted with diethyl ether. The solvent was evaporated in vacuo to leave a residue which was purified by column chromatography (silica gel) employing 1-5% ethyl acetate in hexane as eluents to obtain 3-(4-formyl-phenyl)-propionic acid ethyl ester (0.734 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08889698B2 |
|---|
| Source dataset | uspto-grants-2014_11 |
|---|
| ORD ID | ord-31b131695bb84240b49d7a88697497be |
|---|
| Source note | uspto-grants-2014_11 |
|---|