HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362257Generated: October 26, 2026
Iodoethane → 2-Ethoxy-3-trifluoromethoxybenzaldehyde
https://huagongshe.com/reaction/1362257
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Hydroxy-3-(trifluoromethoxy)benzaldehyde | HCID 2779270 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Ethoxy-3-trifluoromethoxybenzaldehyde | HCID 59277610 | 103.7% |
Reaction Steps
To a solution of 2-hydroxy-3-trifluoromethoxybenzaldehyde (1.00 g, 4.82 mmol) in DMF (10 mL), was added K2CO3 (1.46 g, 10.6 mmol) followed by iodoethane (0.57 mL, 7.24 mmol) and the mixture was heated to 37° C. for 6 h. The reaction was quenched by the addition of H2O (40 mL) and the mixture was extracted with EtOAc (3×100 mL). The combined organics were washed with brine (2×100 mL), dried (Na2SO4) and concentrated to yield the title compound (1.17 g, quant.) as an orange oil: 1H NMR (300 MHz, DMSO-d6) δ 10.31 (s, 1H), 7.77 (m, 2H), 7.38 (t, J=8.1 Hz, 1H), 4.19 (q, J=6.9 Hz, 2H), 1.36 (t, J=6.9 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07879872B2 |
|---|
| Source dataset | uspto-grants-2011_02 |
|---|
| ORD ID | ord-29249f041c0d4bc4839e62a984e08d18 |
|---|
| Source note | uspto-grants-2011_02 |
|---|