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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019752Generated: October 29, 2026

Benzylamine → Benzyl-(3-methoxy-4-nitro-benzyl)amine

https://huagongshe.com/reaction/1019752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
ReactantTriethylamineHCID 8471—
Reactant3-Methoxy-4-nitrobenzyl bromideHCID 12621604—
SolventTetrahydrofuranHCID 8028—
ProductBenzyl-(3-methoxy-4-nitro-benzyl)amineHCID 2204637891%

Reaction Steps

To a solution of 4-(bromomethyl)-2-methoxy-1-nitrobenzene (1.0 g, 4.06 mmol) in THF (15 ml), triethylamine (1.23 g, 12.19 mmol) and benzyl amine (1.3 g, 12.19 mmol) were added at RT and the reaction was stirred for 2 hours. The reaction mixture was partitioned between water (50 ml) and EtOAc (25 ml) and the separated aqueous layer was extracted with EtOAc (15 ml). The combined organic extracts were dried (Na2SO4) and concentrated under reduced pressure. The crude product was purified by column chromatography on neutral silica gel using 15-25% EtOAc in hexane to give the title compound (1.0 g, 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716287B2
Source datasetuspto-grants-2014_05
ORD IDord-34f6a77ac2c04cc8a2edee44b28081cc
Source noteuspto-grants-2014_05