HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 3-(3-Dimethoxymethyl-4-nitrophenoxy)-benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Cyanophenol | HCID 13394 | — |
| Reactant | 5-Fluoro-2-nitrobenzaldehyde | HCID 587090 | — |
| Product | 3-(3-Dimethoxymethyl-4-nitrophenoxy)-benzonitrile | HCID 58625053 | — |
Reaction Steps
A mixture of 3-cyanophenol (0.38 mol) in ethanol (600 mL) was stirred at room temperature and K2CO3 (0.29 mol) was added. 5-fluoro-2-nitrobenzaldehyde (0.18 mol) was added, and the reaction mixture was stirred and refluxed for 4 hours. The solvent was evaporated, and the residue was stirred in water and extracted with CH2Cl2. The organic layer was separated, dried, filtered off and the solvent was evaporated. The residue was triturated under diisopropyl ether, and then the formed solids were filtered off and dried to yield the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08383637B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-1f2124a3aa644c6faf7e1b14e328c3a7 |
| Source note | uspto-grants-2013_02 |