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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2414820Generated: October 25, 2026

Water → 2-(4-Benzyloxy-3-methoxy-phenyl)-vinylamine

https://huagongshe.com/reaction/2414820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactant2-Methoxy-4-(2-nitroethenyl)-1-(phenylmethoxy)benzeneHCID 15828—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Benzyloxy-3-methoxy-phenyl)-vinylamineHCID 57641537—

Reaction Steps

A stirred suspension of LAH (8.0 g, 0.21 mol) in THF (300 mL) is cooled in an ice bath and a solution of 4-benzyloxy-3-methoxynitrostyrene (15.0 g, 52.6 mmol) in THF (300 mL) is added dropwise. The green reaction mixture is allowed to warm to room temperature over 0.5 h, and is then refluxed for 4 h. The grey reaction mixture is treated successively with water (8 mL), 15% aqueous NaOH (8 mL), and water (24 mL). The resulting gray suspension is stirred at 50° C. for 20 min. The resulting yellow suspension is filtered, and the residue is washed with EtOAc. The combined filtrates are evaporated to provide the title compound as yellow oil which is used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06815451B2
Source datasetuspto-grants-2004_11
ORD IDord-a9ea6218e442440e89e5650b0dee9a1d
Source noteuspto-grants-2004_11