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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212848Generated: October 31, 2026

4-(3-Nitro-5-trifluoromethyl-benzoyl)-morpholine → 4-[3-Nitro-5-(trifluoromethyl)benzyl]morpholine

https://huagongshe.com/reaction/2212848

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(3-Nitro-5-trifluoromethyl-benzoyl)-morpholineHCID 21954989—
SolventTetrahydrofuranHCID 8028—
Product4-[3-Nitro-5-(trifluoromethyl)benzyl]morpholineHCID 2195500538%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of morpholin-4-yl-(3-nitro-5-(trifluoromethyl)phenyl)methanone (457 mg, 1.5 mmol) in THF (5 mL) was added dropwise a solution of borane tetrahydrofuran complex solution (3.1 mL, 3.1 mmol) at ambient temperature and the mixture was heated under reflux for 30 minutes, then cooled. The solvent was evaporated. Aqueous HCl (5 mL) was added and the resulting mixture was heated at 100° C. for 1 hour, then cooled and extracted with ether. The acidic aqueous layer was separated, basified to pH 8 with NaOH and extracted with ether. The ether solution was dried over anhydrous Na2SO4. Evaporation of ether provided 168 mg (0.57 mmol) of 4-(3-Nitro-5-trifluoromethylbenzyl)morpholine (38%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105503B2
Source datasetuspto-grants-2006_09
ORD IDord-2dc5f548b37247dab768dac966b2f555
Source noteuspto-grants-2006_09