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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412004Generated: October 23, 2026

Diethyl Ether → 5-Phenylthiophene-2-carbaldehyde

https://huagongshe.com/en/reaction/412004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantSodium CarbonateHCID 10340—
ReactantPhenylboronic AcidHCID 66827—
Reactant5-Bromothiophene-2-carbaldehydeHCID 78428—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
Product5-Phenylthiophene-2-carbaldehydeHCID 17705391.9%

Reaction Steps

5-Bromothiophene-2-carboxaldehyde (1.0 g, 5.2 mmol) is added to a solution of tetrakis(triphenylphosphine)palladium(0) (180 mg, 0.16 mol) in degassed THF (10 mL). The resulting solution is stirred for 5 minutes and then a solution of phenylboronic acid (760 mg, 6.2 mmol) in THF (10 mL) is added followed by aqueous Na2CO3 (2M, 5.2 mL). The mixture is heated at reflux for 24 h. The reaction mixture is allowed to cool, poured into ether, and washed twice with water. The ether layer is dried over Na2SO4 and concentrated in vacuo. The crude product is purified by flash column chromatography (1:1 hexanes/CH2Cl2) to yield 900 mg (91%) of 5-phenylthiophene-2-carboxaldehyde. 1H NMR (300MHz, CDCl3)δ7.38-7.45, 7.65-7.68, 7.73, 9.88.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562816B2
Source datasetuspto-grants-2003_05
ORD IDord-9042e8cf7efe4b88ac999d58addddc10
Source noteuspto-grants-2003_05