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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015945Generated: October 30, 2026

Iodoethane → 3-Chloro-4-ethoxy-5-fluorobenzaldehyde

https://huagongshe.com/reaction/1015945

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantPotassium HydroxideHCID 14797—
Reactant3-Chloro-5-fluoro-4-hydroxybenzaldehydeHCID 2782787—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product3-Chloro-4-ethoxy-5-fluorobenzaldehydeHCID 2011206598%

Reaction Steps

3-Chloro-5-fluoro-4-hydroxybenzaldehyde (1.0 gram, 5.7 mmol) in THF (40 mL) was heated at reflux for 17 hours with KOH (534 mg, 9.5 mmol, 1.7 eq) in water (5 mL) and iodoethane (1 mL, 2.2 eq). The reaction was then transferred to a separatory funnel with water and extracted with methylene chloride (thrice, 150 mL each). The combined organic layers were washed with 10% aqueous HCl (40 mL), dried (MgSO4), and concentrated to a viscous orange liquid to yield 1.13 g of 3-chloro-4-ethoxy-5-fluorobenzaldehyde (98%). 1H-NMR (500 MHz, CDCl3): 9.84 (d, J=1.9 Hz, 1H), 7.71 (t, J=1.6 Hz, 1H), 7.53 (dd, J=1.9, 10.7 Hz, 1H), 4.37-4.32 (m, 2H), 1.47-1.40 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985762B2
Source datasetuspto-grants-2011_07
ORD IDord-64c19d8e636148fa873467541208a3b6
Source noteuspto-grants-2011_07