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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1805507Generated: November 2, 2026

Ethanol → 4-(Benzyloxy)-2-fluoroaniline

https://huagongshe.com/reaction/1805507

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 numberUS08354411B2
Source datasetuspto-grants-2013_01
ORD IDord-2d4e7710151044908abc4dec0b514957
Source noteuspto-grants-2013_01