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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243706Generated: October 26, 2026

Methylamine → 4-Chloro-2-[4-(methylaminomethyl)naphthalen-1-yloxy]benzonitrile fumarate

https://huagongshe.com/reaction/1243706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantFumaric AcidHCID 444972—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant4-Chloro-2-(4-formylnaphthalen-1-yloxy)benzonitrileHCID 21930386—
SolventAcetic acid methanolHCID 10129899—
Product4-Chloro-2-[4-(methylaminomethyl)naphthalen-1-yloxy]benzonitrile fumarateHCID 2193033874.7%

Reaction Steps

4-Chloro-2-(4-formylnaphthalen-1-yloxy)benzonitrile (0.34 g, 1.1 mmol), methylamine (2M in methanol, 2.0 mL, 4.0 mmol) and sodium cyanoborohydride (80 mg, 1.3 mmol) were stirred at ambient temperature in a 1% acetic acid/methanol solution (30 mL) for 18 h. The solvent was removed in vacuo. The residue was treated with 10% sodium carbonate solution and extracted with ethyl acetate. The ethyl acetate layer was separated and fumaric acid (0.12 g, 1.0 mmol) was added. After the solvent was removed in vacuo, the residue was triturated with ethyl acetate overnight, collected by filtration, and dried to give 4-chloro-2-[4-(methylaminomethyl)naphthalen-1-yloxy]benzonitrile fumarate (328 mg, 68%) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07119122B2
Source datasetuspto-grants-2006_10
ORD IDord-9adf8a0de3cf4b348425d3f8d3826db0
Source noteuspto-grants-2006_10