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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798607Generated: October 29, 2026

Benzoyl chloride → 4-(Furan-2-yl)-2,6-dimethoxyphenyl benzoate

https://huagongshe.com/reaction/1798607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
Reactant4-(Furan-2-yl)-2,6-dimethoxyphenolHCID 54350835—
SolventDichloromethaneHCID 6344—
Product4-(Furan-2-yl)-2,6-dimethoxyphenyl benzoateHCID 5843199657%

Reaction Steps

To a solution of 4-(furan-2-yl)-2,6-dimethoxyphenol (1.3 g, 5.9 mmol) in anhydr CH2Cl2 (20 mL) under argon was added Et3N (1.6 mL, 11.5 mmol) then the mixture was cooled over an ice bath. Benzoyl chloride (0.75 mL, 6.4 mmol) was added dropwise and the reaction was stirred for 3 hrs. 10% aqueous NaHCO3 and CH2Cl2 were added, stirred, and the layers were separated. The organics were washed with H2O and saturated aqueous NaHCO3, dried over MgSO4 and concentrated in vacuo. Purification by chromatography (0-25% EtOAc-hexanes) gave 4-(furan-2-yl)-2,6-dimethoxyphenyl benzoate as a light yellow solid (0.54 g isolated from chromatography of approximately half of the crude product; 57% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343970B2
Source datasetuspto-grants-2013_01
ORD IDord-553080d8ee0c49e1bf2db036e0e54590
Source noteuspto-grants-2013_01