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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855247Generated: October 28, 2026

p-Fluorophenethylamine → 5-Tert-butyl-2-{[2-(4-fluoro-phenyl)-ethylamino]-methyl}-phenol

https://huagongshe.com/reaction/855247

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-FluorophenethylamineHCID 4653—
ReactantSodium borohydrideHCID 4311764—
Reactant4-tert-Butyl-2-hydroxybenzaldehydeHCID 13765272—
SolventMethanolHCID 887—
Product5-Tert-butyl-2-{[2-(4-fluoro-phenyl)-ethylamino]-methyl}-phenolHCID 6934234683.2%

Reaction Steps

1.83 g (13 mmol) of 2-(4-fluoro-phenyl) ethyl amine were added to 2.32 g (13 mmol) of 4-tert-butyl-2-hydroxy benzaldehyde dissolved in 130 ml methanol. The reaction mixture was stirred at rt over night under nitrogen. 492 mg (13 mmol) of sodium borohydride were added in portions and the reaction mixture was stirred for 2 h at rt. The solvent was evaporated and the residue was dissolved in DCM. The organic layer was washed with water and with saturated aqueous NaCl solution, dried over sodium sulfate, filtered and the solvent was evaporated. The residue was purified by column chromatography (250 g silica gel; DCM, then DCM/methanol 19:1) to yield 3.26 g (83%) of 5-tert-butyl-2-{[2-(4-fluoro-phenyl)-ethylamino]-methyl}-phenol as a yellow viscous oil. 1H NMR (DMSO-d6, 300 MHz): δ 7.24 (t, 2H), 7.09 (t, 2H), 6.95 (d, 1H), 6.71 (d, 1H), 6.68 (s, 1H), 3.76 (s, 2H), 1.23 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259183B2
Source datasetuspto-grants-2007_08
ORD IDord-91137bb18f114c46b559d461d632ae07
Source noteuspto-grants-2007_08