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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1407146Generated: November 1, 2026

Ethanol → 4-(Benzyloxy)-2-fluoroaniline

https://huagongshe.com/reaction/1407146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium DithioniteHCID 24489—
Reactant4-Benzyloxy-2-fluoro-1-nitrobenzeneHCID 22180704—
SolventWaterHCID 962—
Product4-(Benzyloxy)-2-fluoroanilineHCID 1149980942%

Reaction Steps

A solution of Na2S2O4 (34.8 g, 200 mmol) in H2O (200 mL) was added to a mixture of 4-(benzyloxy)-2-fluoro-1-nitrobenzene (16.0 g, 64.7 mmol), THF (150 mL), and EtOH (150 mL), and the mixture was stirred for 30 min at room temperature. The reaction mixture was poured into water and extracted with AcOEt. The extract was washed with water and brine, dried over MgSO4, and concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography eluting with hexane/AcOEt (1/1) to give the title compound (5.84 g, 42% yield) as a light brown oil: 1H NMR (300 MHz, CDCl3): δ ppm 3.42 (2H, brs), 4.97 (2H, s), 6.60 (1H, ddd, J=1.1, 2.6, 8.7 Hz), 6.67-6.74 (2H, m), 7.28-7.43 (5H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916566B2
Source datasetuspto-grants-2014_12
ORD IDord-b18c65fa7f2d4a4a9712e64c5ee67ed3
Source noteuspto-grants-2014_12