HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481030Generated: October 26, 2026
Acetic Acid → Methyl 2-(o-chlorobenzylidene)-4-(2-phthalimidoethoxy)acetoacetate
https://huagongshe.com/reaction/481030
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 2-Chlorobenzaldehyde | HCID 6996 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Methyl 4-(2-(1,3-dioxoisoindolin-2-yl)ethoxy)-3-oxobutanoate | HCID 22568398 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | Methyl 2-(o-chlorobenzylidene)-4-(2-phthalimidoethoxy)acetoacetate | HCID 69267975 | — |
Reaction Steps
85 g of methyl 4-(2-(phthalimido)ethoxy)acetoacetate was agitated with 31.7 ml of 2-chlorobenzaldehyde and 37 ml of 2-propanol at 20-25° C. The solution of 1.1 ml of piperidine in 14 ml of 2-propanol was added dropwise during 1.5 hour. The mixture was than agitated for 2 hours at the same temperature and for 2 hours at 35-40° C. The mixture was acidified with 1.5 ml of acetic acid, 140 ml of 2-propanol was added and the solution was cooled to 0-5° C. The isopropanolic layer was separated and the organic layer was again washed with 53 ml of 2-propanol. The organic layer, containing the desired product, was evaporated to dryness in order to remove the residual solvent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06653481B2 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-2fcb00f3be4a4459bdbe802ce05bd19e |
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| Source note | uspto-grants-2003_11 |
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