HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1790422Generated: October 26, 2026
Ethylene Glycol → Ethyl 8-benzyl-1,4-dioxa-8-azaspiro[4.5]decane-6-carboxylate
https://huagongshe.com/reaction/1790422
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Ethyl 1-benzyl-4-oxopiperidine-3-carboxylate | HCID 102624 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethyl 8-benzyl-1,4-dioxa-8-azaspiro[4.5]decane-6-carboxylate | HCID 22038236 | 66% |
Reaction Steps
p-Toluenesulfonic acid monohydrate (1.5 g) was added to a solution (600 ml) of ethyl 1-benzyl-4-oxo-3-piperidinecarboxylate (CAS Registry No. 1454-53-1, 44.7 g) and ethylene glycol (100 ml) in toluene and the resultant mixture was heated under reflux overnight. After cooling the mixture to room temperature, ice water (500 ml) and a saturated aqueous solution (300 ml) of sodium bicarbonate were added thereto followed by extraction with ethyl acetate (400 ml) for three times. The organic phase was washed successively with water (200 ml) twice and brine (300 ml) and dried over anhydrous magnesium sulfate. The residue was purified by silica gel column chromatography (hexane/ethyl acetate system) to give the title compound (30.4 g) as a yellow oil (yield: 66%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07071201B2 |
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| Source dataset | uspto-grants-2006_07 |
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| ORD ID | ord-d3ee222fd0f34ea4b9b1ada4fc613bdb |
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| Source note | uspto-grants-2006_07 |
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