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Water → Benzo-1,3-dioxole-5-carbonitrile

HRID 415680
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 415680
[OH:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][C:9]=1[OH:10])[C:5]#[N:6].Br[CH2:12]Br.C(=O)([O-])[O-].[K+].[K+].O>CN(C=O)C>[O:10]1[C:9]2[CH:8]=[CH:7][C:4]([C:5]#[N:6])=[CH:3][C:2]=2[O:1][CH2:12]1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 962WaterHCID 3024DibromomethaneHCID 11430Potassium CarbonateHCID 870653,4-Dihydroxybenzonitrile

Produkt 1

HCID 78136Benzo-1,3-dioxole-5-carbonitrileAusbeute 94,8 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228Dimethylformamide
Lösungsmittel

Reaktionsbedingungen

Temperatur
120 °C

Versuchsvorschrift

To a solution of 3,4 Dihydroxy benzonitrile (5.0 g, 37.0 mmol) in 20 ml of DMF was added dibromomethane (19.25 g, 110.0 mmol) and potassium carbonate (25.50 g, 184.90 mmol). The reaction mixture was heated at 120° C. for 2 h under the nitrogen atmosphere. After the completion of the reaction mixture (TLC monitoring), reaction mixture was cooled to room temperature. Water (50 ml) was added to the reaction mixture and extracted the compound with ethyl acetate (3×100 mL). The combined organic layers were dried over anhydrous Na2SO4, and evaporated to dryness under reduced pressure to give the title compound as yellow solid (5.16 g, 94.8%).

Aufarbeitung

  1. customAfter the completion of the reaction mixture (TLC monitoring), reaction mixture
  2. temperaturewas cooled to room temperature
  3. extractionextracted the compound with ethyl acetate (3×100 mL)
  4. dry with materialThe combined organic layers were dried over anhydrous Na2SO4
  5. customevaporated to dryness under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-9e97fc81c029423e8bd874f5c87f4688
Quelldatensatz
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08088791B2

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