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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1501031Generated: November 1, 2026

N-Methylaniline → Methyl 4-{[methyl(phenyl)amino]methyl}benzoate

https://huagongshe.com/reaction/1501031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylanilineHCID 7515—
ReactantMethyl 4-FormylbenzoateHCID 15294—
ReactantSodium cyanoborohydrideHCID 5003444—
CatalystAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductMethyl 4-{[methyl(phenyl)amino]methyl}benzoateHCID 2882958926%

Reaction Steps

To a solution of methyl 4-formylbenzoate (1 g, 6.1 mmol) and N-methylbenzenamine (650 mg, 6.1 mmol) in methanol (50 mL) was added acetic acid (2 drops) and the mixture was stirred for 0.5 hour. Then sodium cyanoborohydride (660 mg, 10 mmol) was added in portions. The mixture was stirred at room temperature for 24 hours. The mixture was washed with water (50 mL) and extracted with dichloromethane (50 mL). The organic phase was separated and concentrated to give a residue. The residue was purified by column chromatography (petroleum ether/ethyl acetate=1:1) to give methyl 4-((methyl(phenyl)amino)methyl)benzoate (400 mg, 26%) as a yellow oil. LRMS (M+H+) m/z: calcd 255.13. found 255. 1H NMR (300 MHz, CD3OD): δ 7.96-7.32 (m, 2H), 7.33 (d, J=8.4 Hz, 2H), 7.18-7.12 (m, 2H), 6.74-6.60 (m, 3H), 4.60 (s, 2H), 3.88 (s, 3H), 3.02 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206128B2
Source datasetuspto-grants-2015_12
ORD IDord-6704fba61d7345609aeefa08e5461c73
Source noteuspto-grants-2015_12