HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620863Generated: October 29, 2026
Benzyl Chloride → 7-Benzyl-2-methyl-2,7-diazaspiro[4.4]nonane-1,3,8-trione
https://huagongshe.com/reaction/620863
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Methyl-2,7-diazaspiro[4.4]nonane-1,3,8-trione | HCID 4282630 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-Benzyl-2-methyl-2,7-diazaspiro[4.4]nonane-1,3,8-trione | HCID 2868934 | 63.9% |
Reaction Steps
A solution of 1.82 g (10 mmol) of 2-methyl-2,7-diazaspiro[4.4]nonane-1,3,8-trione in 20 ml N,N-dimethylformamide was added gradually under a nitrogen atmosphere to 0.05 g (10.4 mmol) of 50% oil suspension of sodium hydride which had been previously washed twice with toluene and covered with 10 ml N,N-dimethylformamide. After stirring one hour there was added 1.40 g (11 mmol) of benzyl chloride and stirring was continued overnight at room temperature. After concentrating to a small volume in vacuo, the residue was diluted with 40 ml water and extracted twice with dichloromethane. The combined organic phase was washed with water, dried over magnesium sulfate, and evaporated to give a solid. Crystallization from toluene:hexane to afford 1.74 g of 7-benzyl-2-methyl-2,7-diazaspiro[4.4]nonane-1,3,8-trione, mp 157°-158° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04822801 |
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| Source dataset | uspto-grants-1989_04 |
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| ORD ID | ord-0ae3165b711c4abcb44cf973a480c620 |
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| Source note | uspto-grants-1989_04 |
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