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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9639Generated: October 24, 2026

Water → 4-(4-Trifluoromethylphenyl)thiophene-2-carbaldehyde

https://huagongshe.com/en/reaction/9639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
Reactant3-(Trifluoromethyl)phenylboronic acidHCID 2734388—
Reactant3-Bromothiophene-2-carboxaldehydeHCID 2797079—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-(4-Trifluoromethylphenyl)thiophene-2-carbaldehydeHCID 11736954—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 3-bromothiophene-2-carboxaldehyde (2.0 g) and 3-trifluoromethylbenzene boronic acid (2.19 g) in ethylene glycol dimethyl ether (100 ml) was added sodium carbonate (2.9 g), tetrakis(triphenylphosphine) palladium (0) (0.12 g) and water (50 ml). The mixture was heated to 90° C. under nitrogen. After 18 hours the reaction was allowed to cool and was concentrated. The residue was partitioned between water and ethyl acetate; the organic solution was taken and was washed with brine and then dried (MgSO4) and concentrated. The crude material was purified by SPE (Si); the product eluted with neat chloroform to furnish the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091237B2
Source datasetuspto-grants-2006_08
ORD IDord-ffa3f6e62ec945dc861cc1427e46b8f0
Source noteuspto-grants-2006_08