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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228646Generated: October 30, 2026

Water → 3-(Thiophen-3-yl)benzaldehyde

https://huagongshe.com/reaction/2228646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
Reactant3-BromobenzaldehydeHCID 76583—
ReactantThiophene-3-boronic acidHCID 581760—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
Product3-(Thiophen-3-yl)benzaldehydeHCID 454752686%

Reaction Conditions

Temperature80 °C

Reaction Steps

3.11 g of 3-thiopheneboronic acid (0.024 mol) are added to a solution of 3-bromobenzaldehyde (3 g, 0.016 mol) in 1,2-dimethoxyethane (80 ml), followed by addition of aqueous 2N sodium carbonate solution (5.15 g, 0.048 mol) and a catalytic amount of tetrakis(triphenylphosphine)palladium (0.56 g, 4.9 10−4 mol). The reaction mixture is heated at 80° C. for 16 hours and is then cooled to room temperature and poured into water. The resulting mixture is extracted with ethyl acetate and the organic phase is washed with saturated aqueous sodium chloride solution. The organic phase is dried over magnesium sulfate and filtered, and the solvent is evaporated off under reduced pressure. The title product is isolated by chromatography on a column of silica (eluent: 90/10 cyclohexane/ethyl acetate). 2.61 g of a pale yellow solid are recovered.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06417222B1
Source datasetuspto-grants-2002_07
ORD IDord-10b4d6e12b894b6c84fb6830cf10a512
Source noteuspto-grants-2002_07