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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708448Generated: October 26, 2026

Water → 3-Iodo-5-methoxy-4-propoxybenzaldehyde

https://huagongshe.com/reaction/1708448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant1-IodopropaneHCID 33643—
ReactantBenzaldehyde, 4-hydroxy-3-iodo-5-methoxy-HCID 79499—
SolventDimethylformamideHCID 6228—
Product3-Iodo-5-methoxy-4-propoxybenzaldehydeHCID 477010193.4%

Reaction Steps

5-Iodovanillin (25 g, 0.09 mol) in DMF (100 mL) was treated with potassium carbonate (32 g, 0.23 mol) and n-propyl iodide (52 g. 0.3 mol, 31 mL) and heated for 16 hours. The solution was allowed to cool to room temperature and then poured into water (500 mL) and extracted with ether (3×250 mL). The organic layers were combined and washed with water and saturated sodium chloride solution, and then dried over magnesium sulfate. The organic layer was evaporated by distillation under diminished pressure to an oil, and then purified by column chromatography (silica, 7:3 petroleum ether-ethyl acetate), to provide an amber colored solid (26.9 g, 93%). 1H NMR (CDCl3) 1.07 (t, 3H), 1.85 (m, 2H), 3.89 (s, 3H), 4.06 (t, 3H), 7.39 (s, 1 H), 7.84 (s, 1 H), 9.81 (s, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05358938
Source datasetuspto-grants-1994_10
ORD IDord-de010eadbc7c41288d97e06938c6e170
Source noteuspto-grants-1994_10