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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246651Generated: October 26, 2026

Potassium Carbonate → 3-Chloro-5-(2,2,2-trifluoroethoxy)benzaldehyde

https://huagongshe.com/reaction/1246651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthanol, 2,2,2-trifluoro-, 1-(4-methylbenzenesulfonate)HCID 67942—
Reactant3-Chloro-5-hydroxybenzaldehydeHCID 21904648—
SolventDimethylformamideHCID 6228—
Product3-Chloro-5-(2,2,2-trifluoroethoxy)benzaldehydeHCID 8582303362.2%

Reaction Conditions

Temperature110 °C

Reaction Steps

To a magnetically stirred solution of 3-chloro-5-hydroxybenzaldehyde (2.0 g, 12.8 mmol; see Example 1(ii) above) and potassium carbonate (2.3 g, 16.6 mmol) in DMF (35 mL) under nitrogen was added 2,2,2-trifluoroethyl p-toluenesulfonate (4.2 g, 16.6 mmol) at room temperature. The mixture was heated to 110° C. for 7 h and then stirred overnight at room temperature. The reaction was cooled to 0° C., poured into ice-cold 2 N HCl (100 mL) and extracted with EtOAc (2×75 mL). The combined organic extracts were washed with 0.5 N HCl (2×50 mL), dried (Na2SO4), filtered, and concentrated in vacuo. The brown oil was chromatographed on silica gel eluting with Hex:EtOAc (6:1) to afford the sub-title compound (1.9 g, 61%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129233B2
Source datasetuspto-grants-2006_10
ORD IDord-d2a098ef5d564099974b9c6dcff4a468
Source noteuspto-grants-2006_10