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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424635Generated: November 1, 2026

Trifluoroacetic acid → Trifluoroacetic acid

https://huagongshe.com/reaction/1424635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 58137297HCID 58137297—
ProductTrifluoroacetic acidHCID 6422—
ProductHCID 66953374HCID 66953374—

Reaction Conditions

Temperature80 °C

Reaction Steps

Crude 7-chloro-N-(2-adamantyl)-2-(4-methoxybenzyl)-3,3-dimethylspiro[isoindoline-1,4′-piperidine]-1′-carboxamide was dissolved in neat TFA (3 mL) and the mixture was heated to 80° C. for 17 h. After this time LC-MS analysis showed complete removal of the p-methoxybenzyl group. The solution was evaporated the amine purified by prep HPLC to afford 7-chloro-N-(2-adamantyl)-3,3-dimethylspiro[isoindoline-1,4′-piperidine]-1′-carboxamide as its TFA salt. LC-MS Method 1 tR=1.43 min, m/z=428; 1H NMR (CD3OD) δ=7.47 (m, 2H), 7.37 (m, 1H), 4.22 (m, 2H), 3.89 (s, 1H), 3.21 (t, J=12.9, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927715B2
Source datasetuspto-grants-2015_01
ORD IDord-e135ac62bf3d41d5959723be4e9bc79d
Source noteuspto-grants-2015_01