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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921182Generated: October 30, 2026

Trifluoroacetic acid → 1'-(2,2,2-Trifluoroethyl)-spiro[indoline-3,4'-piperidin]-2-one

https://huagongshe.com/reaction/1921182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylamineHCID 8471—
Reactant2,2,2-Trifluoroethyl trifluoromethanesulfonateHCID 80366—
ReactantSpiro(indole-3,4'-piperidin)-2(1H)-oneHCID 18435788—
SolventAcetoneHCID 180—
Product1'-(2,2,2-Trifluoroethyl)-spiro[indoline-3,4'-piperidin]-2-oneHCID 18449358—

Reaction Steps

A mixture of spiro[indoline-3,4′-piperidin]-2-one, [PCT Int. Appl. WO 0145707 A1 (2001)] trifluoroacetic acid salt (3.66 g, 11.6 mmol), 2,2,2-trifluoroethyl trifluoromethanesulfonate (1.63 mL, 11.6 mmol), and triethylamine (8.06 mL, 57.9 mmol) in acetone (30 mL) was heated at reflux for 16 h. The mixture was allowed to cool, and the solvent removed under reduced pressure. The residue was taken up in CH2Cl2 (50 mL) and washed with saturated aqueous NaHCO3 (50 mL). The aqueous layer was further extracted with CH2Cl2 (2×25 mL). The combined organic layers were dried over Na2SO4, filtered, and concentrated in vacuo to give the title compound. MS: m/z=285 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173655B2
Source datasetuspto-grants-2012_05
ORD IDord-54825f58bf794b1d9a186ccccbf68fc7
Source noteuspto-grants-2012_05