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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetone | HCID 6571 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-[(Benzyloxy)carbonyl]azetidine-3-carboxylic acid | HCID 10988214 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Azetidine-1,3-dicarboxylic acid 1-benzyl ester 3-(2-oxo-propyl)ester | HCID 67457562 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09346816B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-3055dc1c5e664f9aa6ee4592c978aaa0 |
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| Source note | uspto-grants-2016_05 |
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