Carbon tetrabromide → 4-(Bromomethyl)benzene-1,2-dicarbonitrile

HRID 1421763Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1421763
O[CH2:2][C:3]1[CH:4]=[C:5]([C:11]#[N:12])[C:6](=[CH:9][CH:10]=1)[C:7]#[N:8].C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.C(Br)(Br)(Br)[Br:33]>C1COCC1>[Br:33][CH2:2][C:3]1[CH:4]=[C:5]([C:11]#[N:12])[C:6](=[CH:9][CH:10]=1)[C:7]#[N:8]

Komponenten

5

Versuchsvorschrift

4-Hydroxymethyl-phthalonitrile from step 2 (1.3 g, 8.2 mmol) was dissolved in THF (41 ml) and treated with Ph3P (3.2 g, 12.3 mmol) followed by CBr4 (4 g, 12.3 mmol). The reaction mixture was stirred at room temp. for 21 hours. The solvent was removed in vacuo and the residue purified by flash chromatography (15% EtOAc/Hexane) to yield the desired product.

Aufarbeitung

  1. customThe solvent was removed in vacuo
  2. customthe residue purified by flash chromatography (15% EtOAc/Hexane)

Quellen und Nachweise

ORD-Eintrag
ord-ca0e1821c093492cbc3d6d390b3e346d
Quelldatensatz
uspto-grants-2000_06
Patentnummer
US06077853

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