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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551960Generated: October 27, 2026

Formaldehyde → Methyl 5-[(4-[(4-butylphenyl)ethynyl]benzyl}(methyl)amino]-2-fluorobenzoate

https://huagongshe.com/reaction/551960

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 5-({4-[(4-butylphenyl)ethynyl]benzyl}amino)-2-fluorobenzoateHCID 11452740—
SolventFormic AcidHCID 284—
ProductMethyl 5-[(4-[(4-butylphenyl)ethynyl]benzyl}(methyl)amino]-2-fluorobenzoateHCID 5755455022.3%

Reaction Steps

A solution of methyl 5-({4-[(4-butylphenyl)ethynyl]benzyl}amino)-2-fluorobenzoate (305 mg; 0.73 mmol), formaldehyde (Aldrich, 50 μl; 1.84 mmol) and formic acid (2.5 mL) was stirred under microwaves at 100° C. for 5 min. The reaction mixture was then poured into an aqueous solution of NaOH 1M and extracted twice with EtOAc. The combined organic layers were washed with brine, dried over magnesium sulfate, filtrated and concentrated. Purification of the crude (257 mg, yellow oil) by flash chromatography on silicagel afforded 70 mg of the title compound as a yellow powder. HPLC, Rt: 5.84. min (purity=100%). 1H NMR (CDCl3) δ: 7.4 (m, 4H), 7.3 (s, 1H), 7.2 (m, 4H), 6.9 (t, J=7.8 Hz, 1H), 6.75 (m, 1H), 4.4 (s, 2H), 2.92 (s, 3H), 2.5 (t, J=7.7 Hz, 2H), 1.5 (m, 2H), 1.25 (m, 2H), 0.8 (t, J=7.53 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947851B2
Source datasetuspto-grants-2011_05
ORD IDord-752b8109fa3748ae8a2565ee647ccc16
Source noteuspto-grants-2011_05