HuagongsheHuagongshe Chemistry Print Report · For research reference only
o-Vanillin → Benzaldehyde, 3-methoxy-2-(4-nitrophenoxy)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | o-Vanillin | HCID 8991 | — |
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Benzaldehyde, 3-methoxy-2-(4-nitrophenoxy)- | HCID 22402430 | 71% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
A mixture of 14.10 g (0.10 mole) of 4-fluoronitrobenzene, 16.40 g (0.10 mole) of o-vanillin, 30 g of powdered potassium carbonate, and 40 mL of DMF is heated with stirring to the boiling point. After 10 minutes the mixture is cooled to 100° C. and 300 mL of ice water is added. Petroleum ether (200 mL) is added and the entire mixture filtered and the cake is washed with 200 mL of water and then 200 mL of petroleum ether. The damp cake slurried in 100 mL of methanol and filtered; wt 19.50 g (71% yield); mp 130°-131° C.; mass spectrum (DEI), 273 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05350757 |
| Source dataset | uspto-grants-1994_09 |
| ORD ID | ord-e4e10bcbf79a4eefb4eb06d7598c3e98 |
| Source note | uspto-grants-1994_09 |