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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 742937Erstellt: 24. Oktober 2026

2-Bromothiophene → 2,2':5',2'',5'',2'''-Quaterthiophene

https://huagongshe.com/de/reaction/742937

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-BromothiopheneHCID 13851—
Edukt5,5'-Dibromo-2,2'-bithiopheneHCID 638908—
EduktMagnesiumHCID 5462224—
EduktHCID 178418438HCID 178418438—
KatalysatorHCID 178418745HCID 178418745—
LösungsmittelDiethyl EtherHCID 3283—
Produkt2,2':5',2'',5'',2'''-QuaterthiopheneHCID 395493—

Reaktionsschritte

Thienylmagnesiumbromide, made from 13 gr (80 mmol) of T-Br and 2.43 gr (100 mmol) of magnesium in 50 ml of anhydrous ether, was added to a solution of 11.71 gr (36 mmol) of 5,5'-dibromo-2,2'-bithiophene and 100 mg (0.18 mmol) of Ni(dppp)Cl2 in 150 ml of ether. The reaction mixture was refluxed for 4 hours and subsequently poured on an ice/dilute hydrochloric acid mixture. The product was extracted with toluene and recrystallized from a mixture of toluene and ethanol. The resulting orange powder was dried in vacuo. Yield: 6,75 gr (20 mmol, 57%) of T4. M.p.: 203° C. (litt: 212). Elemental analysis: found% (theory%) C 56.49 (58.15), H 3.05 (3.05), S 37.0 (38.8). 1H-NMR (300 MHz, CDCl3): ∂=7.23 (2H, dd, J=5.0 and 1.0 Hz), ∂=7.19 (2H, dd, J=3.7 and 1.0 Hz), ∂=7.08 (4H, s), ∂=7.03 (2H, dd, J=5.0 and 3.7 Hz). M/z: 330 D (M.W.=330).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05556524
Quelldatensatzuspto-grants-1996_09
ORD IDord-5c36b1f41c744aadbd163bf24bf25ecd
Quellennotizuspto-grants-1996_09