HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene carbonate → 5-Ethoxy-2-fluoro-4-(2-hydroxy-ethoxy)-benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene carbonate | HCID 7303 | — |
| Reactant | 5-Ethoxy-2-fluoro-4-hydroxy-benzaldehyde | HCID 22647584 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-Ethoxy-2-fluoro-4-(2-hydroxy-ethoxy)-benzaldehyde | HCID 21905578 | 90.8% |
Reaction Steps
The 5-ethoxy-2-fluoro-4-hydroxy-benzaldehyde (9.15 g) described in example 1.3 was dissolved in toluene (80 ml). Ethylene carbonate (5.25 g) and tetrabutylammonium iodide (1.83 g) were added and the mixture was heated to reflux for 22 h. The mixture was cooled to room temperature and filtered over a plug of silica gel. The product was eluted with hexane/ethyl acetate. The solvent was evaporated and the solid was washed with hot hexane to give 10.3 g of 5-ethoxy-2-fluoro-4-(2-hydroxy-ethoxy)-benzaldehyde as a slightly orange solid. MS: 228 ([M]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06548694B2 |
| Source dataset | uspto-grants-2003_04 |
| ORD ID | ord-f731d73c87cb4ed4aedeea270298d89c |
| Source note | uspto-grants-2003_04 |