HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Diethyl (2,6-dimethoxybenzylidene)malonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 2,6-Dimethoxybenzaldehyde | HCID 96404 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Diethyl (2,6-dimethoxybenzylidene)malonate | HCID 12514881 | — |
Reaction Steps
A mixture of 1.52 ml of diethyl malonate, 1.66 g of 2,6-dimethoxybenzaldehyde, 0.1 ml of piperidine, 0.11 ml of glacial acetic acid and 100 ml of toluene was boiled at 110° C. on a water separator for 3.5 hours. The solution was extracted with 10% NaHCO3 solution and back-washed with saturated NaCl solution. The organic phase was dried, filtered under suction and evaporated under reduced pressure. There were obtained 2.8 g of diethyl (2,6-dimethoxybenzylidene)malonate, as a dark yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05270313 |
| Source dataset | uspto-grants-1993_12 |
| ORD ID | ord-9ac6537c309a41c787eebe8636cabbc8 |
| Source note | uspto-grants-1993_12 |