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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497427Generated: November 1, 2026

Sodium Carbonate → 5-(4-methoxyphenyl)thiophene-2-carbaldehyde

https://huagongshe.com/reaction/1497427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant5-Bromothiophene-2-carbaldehydeHCID 78428—
Reactant(4-Methoxyphenyl)boronic acidHCID 201262—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
Product5-(4-methoxyphenyl)thiophene-2-carbaldehydeHCID 2797800—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirred solution of 5-bromothiophene-2-carbaldehyde (1 g, 5.2 mmol) in toluene (40 mL) and ethanol (20 mL) was added (4-methoxyphenyl)boronic acid (1.59 g, 10.4 mmol), 2M Na2CO3 (14.7 mL), and Pd(PPh3)4 (60 mg, 0.05 mmol). The reaction was purged with argon and heated at 60° C. for about 5 h. The reaction mixture was concentrated, diluted with water (100 mL), and extracted with ethyl acetate (2×200 mL). The combined organic extracts were washed with brine solution (20 mL), the organic layer was dried over Na2SO4 and concentrated under vacuum to obtain crude product. The crude product was purified by flash chromatography (silica gel, 60-120μ) using 10% ethyl acetate in hexane eluent to afford 5-(4-methoxyphenyl)thiophene-2-carbaldehyde as off white solid (1 g, 87.7% yield). 1H NMR (400 MHz, DMSO-d6): δ 9.85 (s, 1H), 7.97 (d, 1H), 7.73 (d, 2H), 7.61 (d, 1H), 7.02 (d, 2H), 3.98 (s, 3H); LC-MS m/z calcd for [M+H]+ 219.04. found 219.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199975B2
Source datasetuspto-grants-2015_12
ORD IDord-6fbc05ca68104bac80b0b02d70fb855a
Source noteuspto-grants-2015_12