HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213014Generated: October 30, 2026
Trifluoroacetic acid → 2-Oxa-7-azaspiro[3.5]nonane
https://huagongshe.com/reaction/2213014
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 7-Boc-2-oxa-7-azaspiro[3.5]nonane | HCID 21955210 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Oxa-7-azaspiro[3.5]nonane | HCID 21955284 | 17% |
Reaction Steps
Trifluoroacetic acid (5 mL) was added to a solution of 1,1-dimethylethyl 2-oxa-7-azaspiro[3.5]nonane-7-carboxylate (Description 69, 80 mg, 0.625 mmol) in dichloromethane (15 mL) and the mixture was stirred at room temperature for 3 hours. Saturated aqueous sodium hydrogen carbonate (3 mL) and dichloromethane (5 mL) were added and the layers were separated. The aqueous layer was extracted with dichloromethane (3×3 mL) and the combined organic fractions were poured onto an SCX cartridge (Varian Bond Elut™; 10 mL/500 mg). The cartridge was washed with methanol (4×2 mL), then eluted with methanolic ammonia (2M, 2×2 mL). The solvent was evaporated under reduced pressure to give the title compound as a colorless solid (8 mg, 17%). m/z (ES+) 128 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07105507B2 |
|---|
| Source dataset | uspto-grants-2006_09 |
|---|
| ORD ID | ord-1314d738a66749bb93084e54da55d6f0 |
|---|
| Source note | uspto-grants-2006_09 |
|---|