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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1876609Generated: October 31, 2026

Trifluoroacetic acid → 2,2,2-Trifluoro-1-[7-(phenylmethyl)-4,7-diazaspiro[2.5]oct-4-yl]ethanone

https://huagongshe.com/reaction/1876609

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
Reactant7-Benzyl-4,7-diazaspiro[2.5]octaneHCID 58542325—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
Product2,2,2-Trifluoro-1-[7-(phenylmethyl)-4,7-diazaspiro[2.5]oct-4-yl]ethanoneHCID 58542406102.1%

Reaction Steps

Anhydrous trifluoroacetic acid (8.50 ml, 61.1 mmol) was added dropwise to a methylene chloride (200 ml) solution of the compound (10.3 g, 50.9 mmol) obtained in Step 3 above and triethylamine (17 ml, 122 mmol) with ice cooling and the resulting mixture was stirred at the same temperature for 1 hour. Saturated aqueous sodium bicarbonate solution was added to the reaction mixture, the resulting mixture was diluted with chloroform, washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to give the title compound (15.5 g, 100%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309546B2
Source datasetuspto-grants-2012_11
ORD IDord-546dd40b1bf6455ba49dfd81afdbaa98
Source noteuspto-grants-2012_11