Tosylmethyl isocyanide → 3-(3,4-Dichlorophenyl)-4-nitro-1H-pyrrole

HRID 2209573Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2209573
[Cl:1][C:2]1[CH:3]=[C:4]([CH:10]=[CH:11][C:12]=1[Cl:13])[CH:5]=[CH:6][N+:7]([O-:9])=[O:8].C1(C)C=CC(S([CH2:23][N+:24]#[C-:25])(=O)=O)=CC=1>CS(C)=O.CCOCC.O>[Cl:1][C:2]1[CH:3]=[C:4]([C:5]2[C:6]([N+:7]([O-:9])=[O:8])=[CH:25][NH:24][CH:23]=2)[CH:10]=[CH:11][C:12]=1[Cl:13]

Komponenten

6

Versuchsvorschrift

Sodium hydride (2.66 g of a 60% suspension in oil is rinsed with dry ether; 66 mmol) and suspended in 150 mL of dry ether. To this mixture is added over 15 minutes a mixture of 12.0 g (5.5 mmol) of 3,4-dichloro-β-nitrostyrene and 10.8 g (5.5 mmol) of (p-tolylsulfonyl)methyl isocyanide in 50 mL of DMSO and 150 mL of ether. The mixture is stirred for 1.5 hours and then diluted with 150-200 mL of water and additional ether. The ether layer is separated, dried over magnesium sulfate, and concentrated in vacuo. The resulting 10.6 g of crude product is purified by chromatography on silica gel using a 4:1 mixture of chloroform and ethyl acetate. A 7.2 g solid fraction is recrystallized from chloroform-ethyl acetate-hexane to give 3.0 g of yellow solid, m.p. 187°-188° C. (dec.).

Aufarbeitung

  1. washSodium hydride (2.66 g of a 60% suspension in oil is rinsed with dry ether
  2. additionTo this mixture is added over 15 minutes
  3. customThe ether layer is separated
  4. dry with materialdried over magnesium sulfate
  5. concentrationconcentrated in vacuo
  6. customThe resulting 10.6 g of crude product is purified by chromatography on silica gel using
  7. additiona 4:1 mixture of chloroform and ethyl acetate
  8. customA 7.2 g solid fraction is recrystallized from chloroform-ethyl acetate-hexane

Quellen und Nachweise

ORD-Eintrag
ord-143ac51a609347ac9ff33806b4d6eb1d
Quelldatensatz
uspto-grants-1995_10
Patentnummer
US05455263

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