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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 221058Erstellt: 27. Oktober 2026

Sodium Carbonate → 5-Chloro-2,2'-bithiophene

https://huagongshe.com/reaction/221058

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
Edukt2-Bromo-5-chlorothiopheneHCID 76133—
Edukt2-Thiopheneboronic acidHCID 2733960—
KatalysatorHCID 178418397HCID 178418397—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
Produkt5-Chloro-2,2'-bithiopheneHCID 1250145080,7%

Reaktionsschritte

To a solution of 2-bromo-5-chlorothiophene (4.11 g), thiophene-2-boronic acid (4.00 g), tetrakis(triphenylphosphine)palladium (0) (1.20 g) and 2M aqueous sodium carbonate solution (31.3 ml) in dimethoxyethane (100 ml) was heated under reflux under argon atmosphere for 2.5 hours. The reaction mixture was cooled, and extracted with ethyl acetate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (hexane) to give 2-(5-chloro-2-thienyl) thiophene (3.37 g) as pale yellow oil. (2) The above 2-(5-chloro-2-thienyl)thiophene and 5-bromo-2-methylbenzoic acid obtained in Reference Example 4-(1) were used and treated in a manner similar to Reference Example 5 to give 5-bromo-1-(5-(5-chloro-2-thienyl)-2-thienylmethyl)-2-methylbenzene as a colorless solid. APCI-Mass m/Z 383/385 (M+H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08202984B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-42a2dc9ff65b42988b17141fa24ff97e
Quellennotizuspto-grants-2012_06