HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2066490Generated: October 31, 2026
Trifluoroacetic acid → HCID 86650181, compound
https://huagongshe.com/reaction/2066490
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | tert-Butyl 3-(trifluoroacetyl)-3,8-diazabicyclo[3.2.1]octane-8-carboxylate | HCID 21904733 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86650181 | HCID 86650181 | 66% |
Reaction Steps
To a solution of 3,8-diaza-bicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester (212 mg, 1.0 mmol) in DCM (4 mL) were added triethylamine (208 μL, 1.5 mmol) and trifluoroacetic anhydride (169 μL, 1.2 mmol) at 0° C. and the mixture stirred at 0° C. for 2 h. The reaction mixture was concentrated in vacuo and the resultant residue was purified by column chromatography to give 3-(2,2,2-trifluoro-acetyl)-3,8-diaza-bicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester as a colourless oil. To a solution of 3-(2,2,2-trifluoro-acetyl)-3,8-diaza-bicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester in DCM (4 mL) was added TFA (1 mL) and the solution stirred at RT for 1 h. The reaction mixture was concentrated in vacuo to give the title compound as a colourless oil (212 mg, 66%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08293735B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-90b7ba20644848669e398ea7575bb784 |
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| Source note | uspto-grants-2012_10 |
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