Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006345Generated: October 30, 2026

Ethyl Acetate → HCID 10822693, compound

https://huagongshe.com/reaction/1006345

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium CarbonateHCID 10340—
Reactant5-Bromo-2-methoxybenzaldehydeHCID 90684—
ReactantThiophene-3-boronic acidHCID 581760—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 10822693HCID 1082269381.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

Under nitrogen atmosphere, to a solution of 5-bromo-2-methoxybenzaldehyde (350 mg) in dimethoxyethane (3.5 ml) were added 3-thiopheneboronic acid (417 mg), tetrakis(triphenylphosphine)palladium (0) (282 mg), and 2M sodium carbonate (4.9 ml) at room temperature. After being heated at 80° C. with stirring for 5 hours, the reaction mixture was poured into mixed solvents of ethyl acetate and water. The organic layer was separated, washed with brine, dried over magnesium sulfate, and concentrated under reduced pressure. The resulting residue was purified by column chromatography on silica gel (6 g) using a mixed solvent of hexane and ethyl acetate (10:1). The fractions containing the objective compound were collected and evaporated under reduced pressure to give 2-methoxy-5-(3-thienyl)benzaldehyde (290 mg) as yellowish oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06787543B2
Source datasetuspto-grants-2004_09
ORD IDord-6b0b8d47739d4c7aa85927af5c92dcd8
Source noteuspto-grants-2004_09