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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 640722Generated: October 31, 2026

Acetic Acid → {2-[(2,4-Dimethoxybenzyl)amino]-5-methoxyphenyl}(3-fluorophenyl)methanone

https://huagongshe.com/reaction/640722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant2,4-DimethoxybenzaldehydeHCID 69175—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant(2-Amino-5-methoxyphenyl)(3-fluorophenyl)methanoneHCID 39101631—
Solvent1,1-DichloroethaneHCID 6365—
Product{2-[(2,4-Dimethoxybenzyl)amino]-5-methoxyphenyl}(3-fluorophenyl)methanoneHCID 68659721—

Reaction Steps

To a solution of (2-Amino-5-methoxyphenyl)(3-fluorophenyl)methanone (0.984 g, 4.01 mmol) in 15 mL of dichloroethane was added 4 Å powdered molecular sieves (1 g), followed by sodium triacetoxyborohydride (2.55 g, 12.0 mmol) and acetic acid (0.69 mL, 12.0 mmol). 2,4-Dimethoxybenzaldehyde was added (0.667 g, 4.01 mmol), and the reaction was stirred at room temperature for 3 hours. The reaction was partitioned between EtOAc and saturated NaHCO3 solution, and the organic layer was washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo. The titled product was isolated as a red oil (1.66 g) which was used in the next step without further purification. ESI+ MS: 396.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07692017B2
Source datasetuspto-grants-2010_04
ORD IDord-ea5d159dfb7347a184171b06e49324f0
Source noteuspto-grants-2010_04