Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425294Generated: October 28, 2026

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

https://huagongshe.com/reaction/2425294

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 20112065—

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. 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 numberUS07964624B1
Source datasetuspto-grants-2011_06
ORD IDord-89b1605326734267980f142d9f02d89a
Source noteuspto-grants-2011_06