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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178476Generated: November 2, 2026

Methylamine → 4-Chloro-2-[2-ethoxy-3-(methylaminomethyl)phenoxy]benzonitrile fumarate

https://huagongshe.com/reaction/1178476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantFumaric AcidHCID 444972—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant4-Chloro-2-(2-ethoxy-3-formylphenoxy)benzonitrileHCID 21930382—
SolventEthyl AcetateHCID 8857—
SolventAcetic acid methanolHCID 10129899—
Product4-Chloro-2-[2-ethoxy-3-(methylaminomethyl)phenoxy]benzonitrile fumarateHCID 2193037367.6%

Reaction Steps

4-Chloro-2-(2-ethoxy-3-formylphenoxy)benzonitrile (0.55 g, 1.8 mmol), methylamine (2M in methanol, 3.0 mL, 6.0 mmol) and sodium cyanoborohydride (0.13 g, 2.1 mmol) were stirred at ambient temperature in a 1% acetic acid/methanol solution (55 mL) for 3 days. The solvent was removed in vacuo. The residue was treated with 10% sodium carbonate solution and extracted with ethyl acetate. Fumaric acid (0.21 g, 1.8 mmol) was added to the separated ethyl acetate layer and the solvent removed in vacuo. The residue was triturated overnight with ethyl acetate, collected by filtration, and dried to give 4-chloro-2-[2-ethoxy-3-(methylaminomethyl)phenoxy]benzonitrile fumarate (527 mg, 67%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07276528B2
Source datasetuspto-grants-2007_10
ORD IDord-648a42af66064baf852cde67161219c2
Source noteuspto-grants-2007_10