Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Dimethyl malonate | HCID 7943 | — |
| Reactant | 4-Methoxy-3-(2-phenylethoxy)benzaldehyde | HCID 21716381 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 19606408 | HCID 19606408 | 90.6% |
Reaction Steps
4-Methoxy-3-(2-phenylethoxy)benzaldehyde (51.26 g), dimethyl malonate (26.43 g), piperazine (1.70 g) and acetic acid (1.20 g) were refluxed by heating in 300 ml of benzene under azeotropic dehydration conditions for 8 hours. After the reaction solution was cooled to room temperature, it was washed with water, 1 N hydrochloric acid, a saturated aqueous solution of sodium hydrogencarbonate and a saturated aqueous solution of NaCl in consecutive order and dried over anhydrous magnesium sulfate. The drying agent was separated by filtration and the filtrate was concentrated under reduced pressure. The residue was recrystallized from isopropyl ether-dichloromethane to obtain 67.15 g of methyl 3-[4-methoxy-3-(2-phenylethoxy)phenyl]-2-methoxycarbonylacrylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05990151 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-ba927830fa94426cb3bac56c5922598f |
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| Source note | uspto-grants-1999_11 |
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