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Hydrochloric Acid → 2,2'-Bithiophene, 5-phenyl-

HRID 466914
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 466914
[Mg].Br[C:3]1[S:4][CH:5]=[CH:6][CH:7]=1.Br[C:9]1[S:13][C:12]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[CH:11][CH:10]=1.Cl>CCOCC.[Ni](Cl)Cl.C1(P(C2C=CC=CC=2)CCCP(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>[C:14]1([C:12]2[S:13][C:9]([C:3]3[S:4][CH:5]=[CH:6][CH:7]=3)=[CH:10][CH:11]=2)[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 313Hydrochloric AcidHCID 138512-BromothiopheneHCID 27763132-Bromo-5-phenylthiopheneHCID 5462224Magnesium

Produkt 1

HCID 4547572,2'-Bithiophene, 5-phenyl-Ausbeute 69,4 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 2724937
Dichloro(1,1'-(1,3-propanediyl)bis(1,1-diphenylphosphine-kappaP))nickel
Katalysator
HCID 3283Diethyl EtherLösungsmittel3×

Versuchsvorschrift

In 140 ml of ether, 17.4 g (0.725 mol) of magnesium shavings was reacted according to Grignard with 118 g (0.723 mol) of 2-bromothiophene, and this solution was then introduced into 280 ml of ether, 1.5 g (2.8 mmol) of 1,3-bis(diphenylphosphino)propane nickel dichloride and 140 g (0.586 mol) of 5-bromo-2-phenylthiophene. After the slightly exothermic reaction had subsided, the mixture was stirred for 4 hours at boiling point, and the solution thus obtained was then diluted with 280 ml of ether and stirred into 280 ml of 2N hydrochloric acid solution. The crystals which precipitated out were isolated and dried. There was obtained 98.4 g (69.4% of theory) of 5-phenyl-[2,2'-bithienyl], mp. 116.5°-118° C.

Aufarbeitung

  1. customAfter the slightly exothermic reaction
  2. customthe solution thus obtained
  3. customThe crystals which precipitated out
  4. customwere isolated
  5. customdried

Quellen und Nachweise

ORD-Eintrag
ord-c5032b8eae244781a9d4143b3c8a6f8c
Quelldatensatz
uspto-grants-1992_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05158598

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