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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771812Generated: November 3, 2026

3-(3-Fluorophenyl)-N-(3-hydroxy-2,6-dimethyl-phenyl)-5-methoxy-benzamide → 3-[[3-(3-Fluorophenyl)-5-methoxy-phenyl]methylamino]-2,4-dimethyl-phenol

https://huagongshe.com/reaction/1771812

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(3-Fluorophenyl)-N-(3-hydroxy-2,6-dimethyl-phenyl)-5-methoxy-benzamideHCID 89443728—
SolventTetrahydrofuranHCID 8028—
Product3-[[3-(3-Fluorophenyl)-5-methoxy-phenyl]methylamino]-2,4-dimethyl-phenolHCID 8944384560.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 3-(3-fluorophenyl)-N-(3-hydroxy-2,6-dimethyl-phenyl)-5-methoxy-benzamide (1.2 g, 3.3 mmol, 1.0 eq) in THF (50 mL) at 0° C. under N2 was added a solution of BH3 (1M in THF, 16.0 mL, 16.0 mmol, 5.0 eq) dropwise. The reaction mixture was heated at 60° C. overnight then cooled to room temperature and quenched with water. The aqueous layer was extracted with EtOAc and the combined organic extracts were washed with water and brine, dried (Na2SO4), filtered and evaporated in vacuo. The residue obtained was purified by column chromatography (petroleum ether:EtOAc, 100:1 to 5:1) to give the title compound as a colorless oil (700 mg, 60%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249085B2
Source datasetuspto-grants-2016_02
ORD IDord-e03f5d8dec694dfdbe6317d61748e2af
Source noteuspto-grants-2016_02