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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2285335Generated: October 25, 2026

Acetic Acid → 3,3'-Dibromo-2,2'-bithiophene

https://huagongshe.com/reaction/2285335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
Reactant3,3',5,5'-Tetrabromo-2,2'-bithiopheneHCID 2740586—
CatalystZincHCID 23994—
SolventEthanolHCID 702—
Product3,3'-Dibromo-2,2'-bithiopheneHCID 81908792%

Reaction Steps

3,3′,5,5′-Tetrabromo-2,2′-bithiophene, 10 (15 g, 31.1 mmol) was added in portion within 0.5 h to a refluxing dispersion of zinc powder (7.8 g, 0.12 mol) in 150 mL of ethanol containing 15 mL of water, 72 mL of glacial acetic acid, and 3.1 mL of 3 M HCl. After refluxing for an additional 2 h and then cooling to room temperature, the mixture was filtered and washed three times with ethanol, and the filtrate was collected. The solvent was then removed by evaporation, and 60 mL of H2O was added. The mixture was then extracted with dichloromethane (3×100 mL), and the combined extract was washed with water, dried over anhydrous MgSO4, and filtered. The solvent was removed by evaporation, and the crude product was crystallized from hexane to give colorless crystals of product 9.2 g, 92% yield. 1H NMR (400 MHz, CDCl3, δ) 7.43 (d, J=5.4 Hz, 2H), 7.09 (d, J=5.4 Hz, 2H). 13C NMR (100 MHz, CDCl3, δ) 130.8, 128.8, 127.5, 112.6. MS (FAB): m/z 324.0 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09147848B2
Source datasetuspto-grants-2015_09
ORD IDord-6e668659d41c46e8bc5b28026c6e5244
Source noteuspto-grants-2015_09