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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324441Generated: October 29, 2026

Hydrochloric Acid → Ethyl 5-(3-chlorophenyl)-3-oxopentanoate

https://huagongshe.com/reaction/324441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetoacetateHCID 8868—
Reactant1-(Bromomethyl)-3-chlorobenzeneHCID 69838—
ReactantLithium diisopropylamideHCID 2724682—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 5-(3-chlorophenyl)-3-oxopentanoateHCID 20462750—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of LDA (2.0M solution in heptanes/tetrahydrofuran/ethylbenzene, 500 ml) in tetrahydrofuran (2 L) at 0° C. was added ethyl acetoacetate (62 ml). After 40 min 3-chlorobenzyl bromide (100 g) was added dropwise and the mixture was stirred at 0° C. for 1 hour. The reaction mixture was acidified with 2N HCl and the organic phase was concentrated under reduced pressure. The residue was dissolved in ethyl acetate and washed with water and brine, dried (MgSO4) and evaporated. Purification was by chromatography eluting with 5-10% ethyl acetate in isohexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06218376B1
Source datasetuspto-grants-2001_04
ORD IDord-597121b0d5e947ce86f54bee3d04c4c6
Source noteuspto-grants-2001_04