Methylamine → HCID 21876343, compound

HRID 724176Notes

Reaction equation

HRID 724176 reaction equation
[Cl:1][C:2]1[CH:10]=[C:9]([Cl:11])[C:8]([N+:12]([O-:14])=[O:13])=[CH:7][C:3]=1[C:4](O)=[O:5].S(Cl)(Cl)=O.[CH3:19][NH2:20]>C1(C)C=CC=CC=1>[Cl:1][C:2]1[CH:10]=[C:9]([Cl:11])[C:8]([N+:12]([O-:14])=[O:13])=[CH:7][C:3]=1[C:4]([NH:20][CH3:19])=[O:5]

Participants

5

Conditions

Temperature
80 °C

Procedure

To a solution of 2,4-dichloro-5-nitrobenzoic acid (8 g, 33.9 mmol) in toluene (200 ml) was added thionyl chloride (12.4 ml, 169 mmol) at room temperature. The mixture was stirred at 80° C. for 5 h. The solvent was removed and the residue was dissolved with tetrahydrofurane (60 ml). The mixture was added 40% methylamine (1.4 ml, 33.9 mmol) at 0° C. and the mixture was stirred at room temperature for 2.5 h. The volatile component was removed under reduced pressure, and the residue was extracted with ethyl acetate (100 ml). The organic layer was washed with water (100 ml), brine (100 ml), then dried (Na2SO4). After removal of solvent, the crude product was purified by flash column chromatography eluting with hexane/ethyl acetate (2:1/1:1/1:2) to afford 5.3 g (63%) of the title compound as pale yellow solids.

Workup

  1. customThe solvent was removed
  2. dissolutionthe residue was dissolved with tetrahydrofurane (60 ml)
  3. stirringthe mixture was stirred at room temperature for 2.5 h
  4. customThe volatile component was removed under reduced pressure
  5. extractionthe residue was extracted with ethyl acetate (100 ml)
  6. washThe organic layer was washed with water (100 ml), brine (100 ml)
  7. dry with materialdried (Na2SO4)
  8. customAfter removal of solvent
  9. customthe crude product was purified by flash column chromatography
  10. washeluting with hexane/ethyl acetate (2:1/1:1/1:2)

Sources & evidence

ORD record
ord-e1f339cf2ab24baca019ab6c623f2add
Source dataset
uspto-grants-2006_11
Patent number
US07141580B2

Reaction notes

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