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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528742Generated: November 1, 2026

Chloroacetone → Azetidine-1,3-dicarboxylic acid 1-benzyl ester 3-(2-oxo-propyl)ester

https://huagongshe.com/reaction/528742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetoneHCID 6571—
ReactantSodium hydrideHCID 24758—
Reactant18-Crown-6HCID 28557—
ReactantSodium BicarbonateHCID 516892—
Reactant1-[(Benzyloxy)carbonyl]azetidine-3-carboxylic acidHCID 10988214—
SolventTetrahydrofuranHCID 8028—
ProductAzetidine-1,3-dicarboxylic acid 1-benzyl ester 3-(2-oxo-propyl)esterHCID 67457562—

Reaction Conditions

Temperature60 °C

Reaction Steps

To 321 mg (75% w/w, 1.37 mmol) azetidine-1,3-dicarboxylic acid monobenzyl ester in 10 mL dry THF were added 82 mg NaH (2.05 mmol, 60% dispersion in mineral oil), 182 mg 18-crown-6 (0.68 mmol), 328 μL chloroacetone (4.11 mmol), and the mixture was stirred at 60° C. for 6 hours. After cooling to room temperature, 10 mL 1 M sodium bicarbonate was added and the mixture was extracted with DCM (2×10 mL), the organic layers were combined and dried over Na2SO4. After filtration and evaporation of the solvent the product was purified by column chromatography (silica, heptane-EtOAc 1:1 to EtOAc).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346816B2
Source datasetuspto-grants-2016_05
ORD IDord-3055dc1c5e664f9aa6ee4592c978aaa0
Source noteuspto-grants-2016_05