Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518861Generated: November 3, 2026

Trifluoroacetic acid → 7-[4-Nitro-3-(propan-2-yloxy)phenyl]-1,7-diazaspiro[4.4]nonane

https://huagongshe.com/reaction/518861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantPotassium CarbonateHCID 11430—
Reactant1,7-Diazaspiro[4.4]nonane-1-carboxylic acid, 7-[3-(1-methylethoxy)-4-nitrophenyl]-, 1,1-dimethylethyl esterHCID 86698010—
SolventDichloromethaneHCID 6344—
Product7-[4-Nitro-3-(propan-2-yloxy)phenyl]-1,7-diazaspiro[4.4]nonaneHCID 8669801497.8%

Reaction Steps

0.33 ml of trifluoroacetic acid is added to a solution of 300 mg of 2-methylpropan-2-yl 7-[4-nitro-3-(propan-2-yloxy)phenyl]-1,7-diazaspiro[4.4]nonane-1-carboxylate in 30 ml of dichloromethane. The mixture is stirred at ambient temperature for 15 hours and then 3 ml of trifluoroacetic acid are again added. After stirring for 15 hours, the reaction mixture is run into 50 ml of a saturated potassium carbonate solution. The aqueous phase is extracted three times with 50 ml of dichloromethane. The organic phases are combined, dried over anhydrous magnesium sulfate, filtered and then concentrated to dryness under reduced pressure, so as to give a yellow oil. The residue is purified by chromatography on silica gel, elution being carried out with dichloromethane/methanol (100/0 to 95/5), so as to obtain 221 mg of 7-[4-nitro-3-(propan-2-yloxy)phenyl]-1,7-diazaspiro[4.4]nonane in the form of a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115140B2
Source datasetuspto-grants-2015_08
ORD IDord-4fd56fc34261438f8a7b983376fce421
Source noteuspto-grants-2015_08