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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212843Generated: November 1, 2026

Hydrochloric Acid → HCID 21954972, compound

https://huagongshe.com/reaction/2212843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzoyl PeroxideHCID 7187—
ReactantMorpholineHCID 8083—
ReactantN-bromobutanimideHCID 67184—
Reactant5-Fluoro-2-nitrotolueneHCID 94956—
SolventCarbon TetrachlorideHCID 5943—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21954972HCID 2195497218.7%

Reaction Steps

5-Fluoro-2-nitrotoluene (1.55 g, 10 mmol), N-bromosuccinimide (1.82 g, 10 mmol), and benzoyl peroxide (0.1 g, 0.4 mmol) were dissolved in CCl4 (50 mL), heated at reflux, and irradiated with light (100 W bulb) for 4 hours. The reaction mixture was filtered and concentrated. The residue was dissolved in THF (50 mL). Morpholine (1.9 g, 22 mmol) was added to the THF solution. The mixture was stirred at ambient temperature for 1 hour and then filtered. The solvent of the filtrate was evaporated. The bright orange residue obtained was then mixed with 5% HCl solution (30 mL) and extracted with ethyl acetate (2×25 mL). The aqueous layer was basified with NaOH solution to pH 8 and then extracted with methylene chloride. Both ethyl acetate solution and methylene chloride solution were dried over anhydrous Na2SO4 separately. Evaporation of ethyl acetate solution afforded an orange oil which was recrystallized from hexane:ether solution to yield 450 mg of a yellow solid, 4-(3-methyl-4-nitrophenyl)morpholine (18%), the by-product. Evaporation of methylene chloride solution afforded 660 mg of the desired compound, 4-(5-fluoro-2-nitrobenzyl)morpholine (27.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105503B2
Source datasetuspto-grants-2006_09
ORD IDord-a9c4c93ed2de44f4b1dc5a7c49186bd2
Source noteuspto-grants-2006_09