HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227255Generated: October 26, 2026
Trifluoroacetic acid → 1,3-Dibenzyl-1,4,8-triazaspiro[4,5]decan-2-one
https://huagongshe.com/reaction/227255
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Tert-butyl 1,3-dibenzyl-2-oxo-1,4,8-triazaspiro[4,5]decane-8-carboxylate | HCID 68839424 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1,3-Dibenzyl-1,4,8-triazaspiro[4,5]decan-2-one | HCID 68837942 | — |
Reaction Steps
Trifluoroacetic acid (68.5 g, 601 mmol) was added dropwise at 0° C. to a solution of tert-butyl 1,3-dibenzyl-2-oxo-1,4,8-triazaspiro[4,5]decane-8-carboxylate (13.5 g, 31.0 mmol) in CH2Cl2 (93 ml), and the mixture was stirred at this temperature for 15 min. After warming to RT, the reaction solution was stirred for a further 2.5 h. Subsequently, the reaction solution was adjusted to pH 7 to 8 using NaHCO3 solution, the organic phase was separated off, and the aqueous phase was extracted with CH2Cl2 (2×30 ml). The combined organic phase was dried over Na2SO4, filtered and the solvent was removed by distillation. Workup was carried out by means of column chromatography to give 1,3-dibenzyl-1,4,8-triazaspiro[4,5]decan-2-one in a yield of 7.8 g (75% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07560468B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-2c33aa05b15a480b9b962d6e8d27af12 |
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| Source note | uspto-grants-2009_07 |
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