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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25476Generated: October 25, 2026

Acetic Acid → Methyl 2-(o-chlorobenzylidene)-4-(2-phthalimidoethoxy)acetoacetate

https://huagongshe.com/reaction/25476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant2-ChlorobenzaldehydeHCID 6996—
ReactantPiperidineHCID 8082—
ReactantMethyl 4-(2-(1,3-dioxoisoindolin-2-yl)ethoxy)-3-oxobutanoateHCID 22568398—
SolventIsopropanolHCID 3776—
ProductMethyl 2-(o-chlorobenzylidene)-4-(2-phthalimidoethoxy)acetoacetateHCID 69267975—

Reaction Conditions

Temperature37.5 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858738B2
Source datasetuspto-grants-2005_02
ORD IDord-f4363df668ef423ea1801561f3f5fbda
Source noteuspto-grants-2005_02