Reaktion #1159656

Reaktionsgleichung

HCl

2-chloropropionitrile

1,3-dichloro-5-nitrobenzene

NaOH

→

(±)-2,6-dichloro-α-methyl-4-nitrobenzeneacetonitrile

Ausbeute 40.0%

Lösungsmittel

DMSO

DMSO

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigewas kept below 30° C
2. 2
   workup.ADDITIONpoured out on ice
3. 3
   FiltrationThe precipitate was filtered off
4. 4
   Waschenwashed with H2O
5. 5
   WaschenThe organic solution was washed with H2O
6. 6
   Sonstigedried
7. 7
   Filtrationfiltered
8. 8
   Sonstigethe solvent was evaporated
9. 9
   SonstigeThe residue was purified by column chromatography over silica gel (eluent: CH2Cl2/cyclohexane 70/30)
10. 10
    SonstigeThe pure fractions were collected
11. 11
    Sonstigethe solvent was evaporated

Vorschrift

A mixture of 2-chloropropionitrile (0.2 mole) and 1,3-dichloro-5-nitrobenzene (0.2 mole) in DMSO (50 ml) was added dropwise at RT to a solution of NaOH (1 mole) in DMSO (150 ml) while the temperature was kept below 30° C. The mixture was stirred at RT for 1 hour, then poured out on ice and acidified with HCl. The precipitate was filtered off, washed with H2O and taken up in CH2Cl2. The organic solution was washed with H2O, dried, filtered and the solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent: CH2Cl2/cyclohexane 70/30). The pure fractions were collected and the solvent was evaporated, yielding 19.5 g (40%) of (±)-2,6-dichloro-α-methyl-4-nitrobenzeneacetonitrile (intermediate 1).

Quelle