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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1052162Generated: October 30, 2026

Ethylene Glycol → Benzyl 1,4-dioxa-7-azaspiro[4.4]nonane-7-carboxylate

https://huagongshe.com/reaction/1052162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantTolueneHCID 1140—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant1-N-Cbz-3-pyrrolidinoneHCID 561203—
SolventEthyl AcetateHCID 8857—
ProductBenzyl 1,4-dioxa-7-azaspiro[4.4]nonane-7-carboxylateHCID 15165037—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of benzyl 3-oxopyrrolidine-1-carboxylate (2.00 g), ethane-1,2-diol (2.85 mL), p-toluenesulfonic acid monohydrate (10 mg) and toluene (20 mL) was stirred with heating in a Dean-Stark apparatus at 120° C. for 6 hr. The mixture was allowed to cool to room temperature, diluted with ethyl acetate (10 mL), washed successively with water (5 mL×2) and brine (5 mL), and dried over anhydrous sodium sulfate. Insoluble material was removed by filtration, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (2.1 g) as a pale-yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388195B2
Source datasetuspto-grants-2016_07
ORD IDord-c0b3466aa5474609bcee973876f6439f
Source noteuspto-grants-2016_07