Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850446Generated: October 26, 2026

1-Bromopentane → Pentyl 4-methoxy-3-pentyloxycinnamate

https://huagongshe.com/reaction/850446

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromopentaneHCID 8057—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(3-Hydroxy-4-methoxyphenyl)prop-2-enoic acidHCID 92126—
SolventDimethylformamideHCID 6228—
ProductPentyl 4-methoxy-3-pentyloxycinnamateHCID 54536911217.7%

Reaction Conditions

Temperature90 °C

Reaction Steps

3-Hydroxy-4-methoxycinnamic acid (9.7 g, 0.050 mol, 1.0 eq) was dissolved in DMF (90 ml). 1-Bromopentane (22.7 g, 0.150 mol, 3.0 eq) and anhydrous potassium carbonate (41.5 g, 0.30 mol, 6.0 eq) were successively added to this solution, and the mixture was stirred under heating at 90° C. for 3 hours. This reaction mixture was cooled to room temperature, and anhydrous potassium carbonate was filtered off. Water (200 ml) was added to the filtrate, and the mixture was exracted twice with ethyl acetate (200 ml). The organic layers were combined, washed with saturated brine (300 ml) and dried over anhydrous sodium sulfate. The drying agent was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by column chromatography (n-hexane/ethyl acetate=15/1-10/1) to give pentyl 4-methoxy-3-pentyloxycinnamate (18.2 g, 100%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06017919
Source datasetuspto-grants-2000_01
ORD IDord-d0b1d754534f478bbff696545eb58029
Source noteuspto-grants-2000_01