HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594274Generated: November 2, 2026
Diethyl Ether → 2-Ethoxy-3-fluorobenzaldehyde
https://huagongshe.com/reaction/594274
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Fluorosalicylaldehyde | HCID 587788 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Ethoxy-3-fluorobenzaldehyde | HCID 86695616 | — |
Reaction Steps
A mixture of commercially available 3-fluoro-2-hydroxybenzaldehyde (5.000 g; 35.70 mmol), iodoethane (11.131 g; 71.40 mmol), and K2CO3 (5.918 g; 42.80 mmol) in anh. DMF (100 ml) was heated to 80° C., under nitrogen, for 3 h. Et2O was added and the organic layer was washed with water, dried over anh. MgSO4, filtered, and concentrated to dryness under reduced pressure affording 2-ethoxy-3-fluorobenzaldehyde as a yellow oil. LC-MS (conditions A): tR=0.74 min.; no ionisation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242970B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-2fccbf003a4a4f06ba946e967502afa4 |
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| Source note | uspto-grants-2016_01 |
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