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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725125Generated: November 4, 2026

2-Chloro-1-(3-fluoro-benzyloxy)-4-nitro-benzene → 3-Chloro-4-(3-fluorobenzyloxy)aniline

https://huagongshe.com/reaction/1725125

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-1-(3-fluoro-benzyloxy)-4-nitro-benzeneHCID 7059269—
CatalystPlatinumHCID 23939—
SolventMethanolHCID 887—
Product3-Chloro-4-(3-fluorobenzyloxy)anilineHCID 705926383%

Reaction Steps

2-Chloro-1-(3-fluoro-benzyloxy)-4-nitro-benzene (4.08 g, 14.5 mmol) is suspended in MeOH (50 ml) and treated wet 5% Pt/C (Degussa type, Aldrich, 1.5 g). The flask is flushed with hydrogen gas from a balloon and the reaction mixture is stirred under hydrogen atmosphere until reaction is judged complete by this-layer chromatography (approximately 2 hours). The reaction mixture is filtered through a Celite plug and the solvent is removed under reduced pressure. The crude product is redissolved in DCM, dried (MgSO4) and concentrated to yield 3.1 g (12 mmol, 83%) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07488823B2
Source datasetuspto-grants-2009_02
ORD IDord-fff70774f73d4013ab522fdc3ef7ea94
Source noteuspto-grants-2009_02