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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178488Generated: October 26, 2026

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

https://huagongshe.com/reaction/1178488

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 numberUS07276528B2
Source datasetuspto-grants-2007_10
ORD IDord-c90d8803de044cb6b6d84e554009eac6
Source noteuspto-grants-2007_10