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Stannous Chloride → 4-Bromo-2-ethoxyaniline

HRID 1480840
Notes
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Reaction equation

HRID 1480840 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-])=O)=[C:4]([O:11][CH2:12][CH3:13])[CH:3]=1.[Sn](Cl)Cl>CCO>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([NH2:8])=[C:4]([O:11][CH2:12][CH3:13])[CH:3]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 24479Stannous ChlorideHCID 155555014-Bromo-2-ethoxy-1-nitrobenzene

Product 1

HCID 155555024-Bromo-2-ethoxyanilineYield 82%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Conditions

Temperature
70 °C

Procedure

To a solution of 4-bromo-2-ethoxy-1-nitrobenzene (Preparation 100, 250 mg, 1.016 mmol) in EtOH (15 mL) was added tin (II) chloride (963 mg, 5.08 mmol). The reaction mixture was heated to 70° C. for 2 hours. The reaction mixture was diluted with ice-water (10 mL) and concentrated in vacuo. Aqueous Na2CO3 (2M, 20 mL) was added and the reaction mixture was extracted with EtOAc (3×20 mL). The combined organic layers were washed with brine (30 mL), dried (MgSO4) and concentrated in vacuo. The residue was purified by passage through a SCX-2 cartridge eluting with 100% MeOH—1M NH3 in MeOH to give the title compound (179 mg, 82%).

Workup

  1. concentrationconcentrated in vacuo
  2. additionAqueous Na2CO3 (2M, 20 mL) was added
  3. extractionthe reaction mixture was extracted with EtOAc (3×20 mL)
  4. washThe combined organic layers were washed with brine (30 mL)
  5. dry with materialdried (MgSO4)
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified by passage through a SCX-2 cartridge
  8. washeluting with 100% MeOH—1M NH3 in MeOH

Sources & evidence

ORD record
ord-747baf79925042a3bc13a5cdebccc696
Source dataset
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09409907B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes