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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1770461Generated: November 1, 2026

3-Furaldehyde → HCID 60208913, compound

https://huagongshe.com/reaction/1770461

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-FuraldehydeHCID 10351—
Reactant4-MethoxybenzylamineHCID 75452—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductHCID 60208913HCID 60208913—

Reaction Steps

A mixture of 3-Furaldehyde (5 mmol, 437 μL) and (4-methoxyphenyl)methanamine in MeOH (20 mL) was stirred at ambient temperature overnight then sodium borohydride (300 mg, 7.89 mmol) was slowly added. The resulting mixture was stirred at room temperature for 15 minutes and quenched with NaOH (1 N, aq). Methanol was removed in vacuo and the resulting slurry was redissolved in ethyl acetate then, washed with water, brine, dried over sodium sulfate and concentrated. Purification by silica gel chromatography (Ethyl acetate:Hexanes 7:3) gave 1-(furan-3-yl)-N-(4-methoxybenzyl)methanamine as an oil. MS (M+H, 218.10); 1H NMR (400 MHz, CDCl3): δ, ppm: 3.64 (s, 2H), 3.74 (s, 2H), 3.80 (s, 3H), 6.39 (m, 1H), 6.86 (m, 1H), 6.88 (m, 1H), 7.23 (m, 1H), 7.25 (m, 1H), 7.35 (m, 1H), 7.38 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09247759B2
Source datasetuspto-grants-2016_02
ORD IDord-2d5f854ee4e54fb4ac00589d832cbe4c
Source noteuspto-grants-2016_02