HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Diethyl 2-(3,4-dimethoxybenzylidene)malonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Veratraldehyde | HCID 8419 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Product | Diethyl 2-(3,4-dimethoxybenzylidene)malonate | HCID 335552 | — |
Reaction Steps
3,4-dimethoxybenzaldehyde (Veratraldehyde) (9.13 g, 55 mM) was heated with malonic acid diethyl ester (8.00 g, 50 mM), acetic acid (0.29 ml) and piperidine (0.74 ml) in benzene (100 ml) in an apparatus equipped with a water separator (Dean-Stark tube) until 50 mM water was separated. After washing the benzene solution with water, it was dried over anhydrous magnesium sulfate. After drying, benzene was evaporated under reduced pressure to obtain a crude product (15.40 g). The crude product thus obtained is pure enough, and can be used in the subsequent reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08106053B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-47ee0ab220f04305ba10fa44f3dc9857 |
| Source note | uspto-grants-2012_01 |