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Stannous chloride dihydrate → 3-Chloro-4-ethylaniline

HRID 1857431
Notes
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Reaction equation

HRID 1857431 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([N+:10]([O-])=O)[CH:5]=[CH:6][C:7]=1[CH2:8][CH3:9].O.O.Cl[Sn]Cl>>[Cl:1][C:2]1[CH:3]=[C:4]([CH:5]=[CH:6][C:7]=1[CH2:8][CH3:9])[NH2:10]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 61436Stannous chloride dihydrateHCID 41134491-Chloro-2-ethyl-5-nitrobenzene

Product 1

HCID 211899483-Chloro-4-ethylanilineYield 98%

Procedure

A solution of 8.9 g (48 mmol) of 31 and 54.6 g (241 mmol) of SnCl2.2H2O in 100 mL of absolute alcohol was refluxed for 1 h. It was evaporated to remove most of the solvent and the residue was treated with 2N NaOH to pH=9. The mixture was filtered and the solid was washed with methanol (10 mL) and ethyl acetate (200 mL). The filtrate was separated and the aqueous phase was extracted with ethyl acetate (2×50 mL). The combined organic solution was dried (MgSO4) and evaporated to leave 7.31 g (98%) of liquid. 1H NMR (CDCl3), 1.178 (t, 3, J=7.5), 2.639 (q, 2, J=7.4), 6.532 (dd, 1, J=2.2, 8.1), 6.700 (d, 1, J=2.2), 6.996 (d, 1, J=8.2).

Workup

  1. customIt was evaporated
  2. custom
to remove most of the solvent
  • additionthe residue was treated with 2N NaOH to pH=9
  • filtrationThe mixture was filtered
  • washthe solid was washed with methanol (10 mL) and ethyl acetate (200 mL)
  • customThe filtrate was separated
  • extractionthe aqueous phase was extracted with ethyl acetate (2×50 mL)
  • dry with materialThe combined organic solution was dried (MgSO4)
  • customevaporated
  • Sources & evidence

    ORD record
    ord-1b898e2fbfe345118ecef498e6157780
    Source dataset
    uspto-grants-2000_11
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US06147075

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes