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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2089680Generated: October 30, 2026

2-Chloroethanol → 2-Fluoro-3-(2-hydroxyethoxy)-5-methoxybenzaldehyde

https://huagongshe.com/reaction/2089680

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloroethanolHCID 34—
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Fluoro-3-hydroxy-5-methoxybenzaldehydeHCID 59495309—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-Fluoro-3-(2-hydroxyethoxy)-5-methoxybenzaldehydeHCID 86677408—

Reaction Conditions

Temperature100 °C

Reaction Steps

Under nitrogen atmosphere, a mixture of 2-fluoro-3-hydroxy-5-methoxybenzaldehyde (17.01 g, 100 mmol), 2-chloroethanol (8.72 mL, 130 mmol), sodium iodide (19.49 g, 130 mmol), potassium carbonate (17.97 g, 130 mmol), and N,N-dimethylformamide (85 mL) was stirred at 100° C. for 4.25 hours, after which 2-chloroethanol (4.70 mL, 70 mmol), sodium iodide (10.49 g, 70 mmol), potassium carbonate (9.68 g, 70 mmol), and N,N-dimethylformamide (17 mL) were added thereto, and the resulting mixture was stirred at the same temperature for 4.25 hours. To the mixture, 2-chloroethanol (2.01 mL, 30 mmol), sodium iodide (4.50 g, 30 mmol), and potassium carbonate (4.15 g, 30 mmol) were added, and the resulting mixture was stirred at 100° C. for 7 hours, after which 2-chloroethanol (2.01 mL, 30 mmol) was added thereto, and the resulting mixture was stirred at the same temperature for 2.5 hours. After cooling the mixture, ethyl acetate and water were added to the reaction mixture, and the resulting mixture was extracted. The organic layer was washed with water and concentrated under reduced pressure to obtain a crude product containing the captioned compound (17.70 g) as a red-brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436009B2
Source datasetuspto-grants-2013_05
ORD IDord-2125abc69cb24bdfa74486aee9ad507f
Source noteuspto-grants-2013_05