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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 1-N-Cbz-3-pyrrolidinone | HCID 561203 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Benzyl 1,4-dioxa-7-azaspiro[4.4]nonane-7-carboxylate | HCID 15165037 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09388195B2 |
|---|
| Source dataset | uspto-grants-2016_07 |
|---|
| ORD ID | ord-c0b3466aa5474609bcee973876f6439f |
|---|
| Source note | uspto-grants-2016_07 |
|---|