HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594271Generated: October 31, 2026
Diethyl Ether → 6-Ethoxy-2,3-difluorobenzaldehyde
https://huagongshe.com/reaction/594271
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,3-Difluoro-6-hydroxybenzaldehyde | HCID 21221031 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Ethoxy-2,3-difluorobenzaldehyde | HCID 10726194 | — |
Reaction Steps
A mixture of commercially available 2,3-difluoro-6-hydroxybenzaldehyde (3.000 g; 21.40 mmol), iodoethane (6.679 g; 42.80 mmol), and K2CO3 (3.551 g; 25.70 mmol) in anh. DMF (60 ml) was heated to 80° C., under nitrogen, for 1.5 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 6-ethoxy-2,3-difluorobenzaldehyde as a yellow solid. LC-MS (conditions A): tR=0.72 min.; no ionisation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09242970B2 |
|---|
| Source dataset | uspto-grants-2016_01 |
|---|
| ORD ID | ord-0a7b9d0a640c4531874a3c38eb146a0a |
|---|
| Source note | uspto-grants-2016_01 |
|---|