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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228648Generated: October 31, 2026

Water → 2-Hydroxy-5-(thiophen-3-yl)benzaldehyde

https://huagongshe.com/reaction/2228648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCesium fluorideHCID 25953—
Reactant5-BromosalicylaldehydeHCID 72863—
ReactantThiophene-3-boronic acidHCID 581760—
CatalystHCID 178418397HCID 178418397—
SolventMethanolHCID 887—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-Hydroxy-5-(thiophen-3-yl)benzaldehydeHCID 20099803—

Reaction Conditions

Temperature80 °C

Reaction Steps

0.15 g of tetrakis(triphenylphosphine)palladium catalyst (1.3 10−4 mol) is added to a solution of 5-bromosalicylaldehyde (0.86 g, 0.0043 mol) and of 3-thiopheneboronic acid (0.6 g, 0.0047 mol) in 10 ml of 1,2-dimethoxyethane and 5 ml of methanol. 1.3 g of cesium fluoride are added and the mixture is heated at 80° C. for 20 hours. The reaction mixture is cooled to room temperature and poured into water. The resulting mixture is extracted with dichloromethane and the organic phase is washed with saturated aqueous sodium chloride solution. The organic phase is dried over magnesium sulfate, filtered and concentrated under reduced pressure. The title product is isolated by chromatography on a column of silica (eluent: 88/12 cyclohexane/ethyl acetate. 0.62 g of a pale yellow solid is recovered.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06417222B1
Source datasetuspto-grants-2002_07
ORD IDord-a181cd352cf147818d2ec63bbeb70432
Source noteuspto-grants-2002_07