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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359629Generated: October 28, 2026

Sodium Carbonate → HCID 14551988, compound

https://huagongshe.com/reaction/1359629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-Bromo-5-chlorothiopheneHCID 76133—
Reactant5-Formyl-2-thiopheneboronic acidHCID 2773430—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
ProductHCID 14551988HCID 1455198824%

Reaction Conditions

Temperature85 °C

Reaction Steps

In a flask are placed 2-bromo-5-chlorothiophene (0.55 mL, 5.0 mmol) and Pd(PPh3)4 (0.17 g, 0.15 mmol), and the flask is vacuum purged and nitrogen filled (3×). THF (10 mL) is added by syringe and stirred 10 min. In a separate flask is placed 5-formyl-2-thiopheneboronic acid (0.94 g, 6.0 mmol) and EtOH (2 mL) and stirred until dissolved. This mixture is added by syringe to the first flask followed by vacuum purge and nitrogen fill (3×). A solution of Na2CO3 (2M, 5.0 mL, 10.0 mmol) is added by syringe followed by vacuum purge and nitrogen fill (3×). The reaction mixture is heated at 85° C. for 20 h. The reaction is cooled to rt and diluted with water. The aqueous solution is extracted with ether (3×). The combined ether layers are washed with water (3×) then brine (2×). The ether is dried over MgSO4, filtered, and concentrated. The crude product is purified over silica gel (5% EtOAc-heptane) to provide the product as an orange solid (0.27 g, 24%). 1NMR (400 MHz, CDCl3) δ 9.89, 7.69, 7.20, 7.16, 6.93.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06599916B2
Source datasetuspto-grants-2003_07
ORD IDord-ae448dfe6bf94d8d8b3c3155395a27a1
Source noteuspto-grants-2003_07