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Potassium Carbonate → 1-Ethynyl-4-iodobenzene

HRID 18349
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 18349
[I:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]#[C:9][Si](C)(C)C)=[CH:4][CH:3]=1.C([O-])([O-])=O.[K+].[K+]>CO>[C:8]([C:5]1[CH:6]=[CH:7][C:2]([I:1])=[CH:3][CH:4]=1)#[CH:9]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 11430Potassium CarbonateHCID 11808725(4-Iodophenylethynyl)trimethylsilane

Produkt 1

HCID 121608331-Ethynyl-4-iodobenzeneAusbeute 64,8 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

To a solution of ((4-iodophenyl)ethynyl)trimethylsilane (5) (2.07 g, 6.23 mmol) in methanol (40 mL) was added K2CO3 (8.0 g, 57.9 mmol) and the reaction was allowed to stir for 48 hours. The volatiles were then removed in vacuo and the residue partitioned between ethyl acetate and H2O. The layers were separated and the aqueous phase re-extracted with ethyl acetate (2×). The combined organic layers were washed (H2O, brine), dried (Na2SO4), and filtered. The solvent was removed in vacuo and the residue was crystallized from hexane at −20° C. (in 2 crops) to give 1-ethynyl-4-iodobenzene (6) as a colorless solid (0.92 g, 64%). 1H NMR (400 MHz, DMSO-d6) δ 7.66 (app d, J=8.6 Hz, 2H), 7.20 (app d, J=8.5 Hz, 2H), 1.54 (s, 1H).

Aufarbeitung

  1. customThe volatiles were then removed in vacuo
  2. customthe residue partitioned between ethyl acetate and H2O
  3. customThe layers were separated
  4. extractionthe aqueous phase re-extracted with ethyl acetate (2×)
  5. washThe combined organic layers were washed (H2O, brine)
  6. dry with materialdried (Na2SO4)
  7. filtrationfiltered
  8. customThe solvent was removed in vacuo
  9. customthe residue was crystallized from hexane at −20° C. (in 2 crops)

Quellen und Nachweise

ORD-Eintrag
ord-b4dda8d4d4954a57bf5cb0599e52ff3b
Quelldatensatz
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07741347B2

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