HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → 1-Bromo-5-ethoxy-2,4-difluorobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Bromo-2,4-difluorophenol | HCID 9834300 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-Bromo-5-ethoxy-2,4-difluorobenzene | HCID 57942661 | 72% |
Reaction Steps
To 97C (2.0 g, 10 mmol) in acetone (30 mL) was added K2CO3 (4.1 g) and iodoethane (2.4 mL). The mixture was stirred at rt overnight. After TLC (10% EtOAc/Hexane) indicated the reaction was complete, the mixture was diluted with diethyl ether, washed with water and brine. The organic layer was dried over MgSO4 and concentrated to give 97D as an colorless oil (1.7 g, 72% yield). 1H NMR (400 MHz, CDCl3) δ ppm 1.44 (t, J=7.03 Hz, 3H) 4.07 (q, J=7.03 Hz, 2H) 6.94 (dd, J=10.77, 8.13 Hz, 1H) 7.11 (dd, J=8.35, 6.59 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07622585B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-62ec20892dbd4dddaba0b538da229b11 |
| Source note | uspto-grants-2009_11 |