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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397625Generated: October 29, 2026

Toluene → 3-Cyclopentyloxy-4-methoxybenzaldehyde

https://huagongshe.com/reaction/397625

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantBromocyclopentaneHCID 8728—
ReactantPotassium CarbonateHCID 11430—
ReactantIsovanillinHCID 12127—
CatalystPotassium IodideHCID 4875—
SolventDimethylformamideHCID 6228—
Product3-Cyclopentyloxy-4-methoxybenzaldehydeHCID 273589380.5%

Reaction Conditions

Temperature65 °C

Reaction Steps

A solution of 100 g (0.66 mol) of isovanillin, 136.2 g (0.99 mol) of anhydrous potassium carbonate, and 3 g of potassium iodide in 650 ml of anhydrous dimethylformamide was stirred at 65° C. 127.3 g (0.85 mol) of cyclopentyl bromide was slowly added dropwise for 1 hour to the solution. This solution was stirred at 65° C. for 1 day and, then, its temperature was lowered to a room temperature. It was diluted by 2.0 L of toluene and was washed with 1M sodium hydroxide (2×1.5 L). The aqueous layer was extracted with 0.5 L of toluene, and the organic layer was washed with distilled water (2×1.5 L). The organic layer was dried and concentrated to obtain 117 g of light brown oily title compound. 1H NMR(CDCl3,d): 9.84(s, 1H) 7.42(m, 2H) 6.95(d, 1H, J=9 Hz) 4.87(m, 1H) 3.93(s, 3H) 2.1-6(m, 8H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610715B1
Source datasetuspto-grants-2003_08
ORD IDord-e0c6ed9e7b1e44eab57367786f177a88
Source noteuspto-grants-2003_08