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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795102Generated: October 25, 2026

Water → 2-Formylphenyl 4-(trifluoromethyl)benzenesulfonate

https://huagongshe.com/reaction/1795102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSalicylaldehydeHCID 6998—
ReactantEthyl AcetateHCID 8857—
Reactant4-(Trifluoromethyl)benzenesulfonyl chlorideHCID 2777399—
SolventPyridineHCID 1049—
Product2-Formylphenyl 4-(trifluoromethyl)benzenesulfonateHCID 2218567152.3%

Reaction Steps

A solution of 4-(trifluoromethyl)benzenesulphonyl chloride (2.4 g, 9.84 mmol) in pyridine (40 mL) is cooled to 0° C. Salicylaldehyde (1.44 g, 11.8 mmol) is added and stirred overnight. Water and ethyl acetate are added to the reaction and shaken. The organic layer is washed with dilute HCl (0.1 N×2), H2O, bicarbonate solution, H2O and dried with sodium sulfate. The organic layer is evaporated to dryness to give a yellow solid, which is recrystallized from ether/hexane to give 2-formylphenyl 4-(trifluoromethyl)benzenesulfonate as a yellow powder (1.70 g, 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07026339B2
Source datasetuspto-grants-2006_04
ORD IDord-fd21f148b6254d80a3e6df1b59f886b1
Source noteuspto-grants-2006_04