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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505015Generated: October 25, 2026

Potassium Carbonate → 3-Chloro-5-(2-fluoroethoxy)benzaldehyde

https://huagongshe.com/reaction/505015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-FluoropropanesulfonateHCID 132622—
Reactant3-Chloro-5-hydroxybenzaldehydeHCID 21904648—
SolventDimethylformamideHCID 6228—
Product3-Chloro-5-(2-fluoroethoxy)benzaldehydeHCID 8582306471.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 3-chloro-5-hydroxybenzaldehyde (8.2 g, 52.5 mmol; see Preparation A(ii) above) and potassium carbonate (9.4 g, 68.2 mmol) in DMF (10 mL) under nitrogen was added a solution of (2-monofluoroethyl) methanesulfonate (9.7 g, 68.2 mmol; see step (i) above) in DMF (120 mL) dropwise at room temperature. The mixture was heated to 100° C. for 5 h and then stirred overnight at room temperature. The reaction was cooled to 0° C., poured into ice-cold 2N HCl and extracted with EtOAc. The combined organic extracts were washed with brine, dried (Na2SO4), filtered and concentrated in vacuo. The brown oil was chromatographed on silica gel eluting with Hex:EtOAc (4:1) to afford the sub-title compound (7.6 g, 71%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781424B2
Source datasetuspto-grants-2010_08
ORD IDord-aaa5e9b19f9f4a2293211a79094d275c
Source noteuspto-grants-2010_08