HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → Methyl 3-(2,4-dimethoxyphenyl)prop-2-enoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 2,4-Dimethoxybenzaldehyde | HCID 69175 | — |
| Reactant | HCID 178525632 | HCID 178525632 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Methyl 3-(2,4-dimethoxyphenyl)prop-2-enoate | HCID 54162205 | — |
Reaction Steps
A mixture of 105.6 g of 2,4-dimethoxybenzaldehyde, 93.6 g of methyl potassium malonate, 200 ml of pyridine (dried over KOH), 1.2 ml of piperidine, 36 ml of acetic acid and 48 g of 3A molecular sieves is heated at 150° C. until evolution of CO2 has ceased. The solution is poured onto ice while hot, and the mixture is acidified to pH 1-2 with concentrated hydrochloric acid and then stirred in the ice bath for 20 minutes. The precipitate is filtered off with suction, washed with 1N HCl and water and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05124478 |
| Source dataset | uspto-grants-1992_06 |
| ORD ID | ord-1059b7c7016645dcae8dbc833471c11b |
| Source note | uspto-grants-1992_06 |