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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401582Generated: October 30, 2026

Hydrochloric Acid → 2-Chloro-3-(5-fluoro-2-methoxy-phenyl)-propionaldehyde

https://huagongshe.com/reaction/401582

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcroleinHCID 7847—
Reactant5-Fluoro-2-methoxyanilineHCID 223105—
ReactantCalciumoxideHCID 6850728—
ReactantSodium NitriteHCID 23668193—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product2-Chloro-3-(5-fluoro-2-methoxy-phenyl)-propionaldehydeHCID 58033095—

Reaction Steps

A solution of sodium nitrite (36 g, 0.51 mole) in water (50 mL) was slowly added to a solution of 5-fluoro-2-methoxy-phenylamine (61.5 g, 0.48 mol) in hydrochloric acid (20% aqueous solution, 115 mL) at 0° C. After stirring for 10 minutes, a cooled (0° C.) solution of acrolein (50 mL, 0.75 mol) in acetone (100 mL) containing calcium oxide (0.56 g, 0.010 mol) was added slowly to the reaction mixture. This was then followed by a solution of cuprous chloride (5 g, 0.05 mol) in acetone (100 mL) containing hydrochloric acid (20% aqueous solution, 10 mL). The mixture was stirred at 0 to 30° C. for 3 hours, and then extracted three times with dichloromethane (300 mL). The combined organic layers were washed with a saturated aqueous solution of sodium bicarbonate, a saturated aqueous solution of sodium chloride, dried over sodium sulfate, filtered, and evaporated to dryness to give a black viscous oil. The crude product was passed through a short silica column to give the crude product, which was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741939B2
Source datasetuspto-grants-2014_06
ORD IDord-99df5ff06f3b4bad850d8a4ad5d395a5
Source noteuspto-grants-2014_06