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Formic Acid → 2-(beta-Methoxyethyl)amino-6-(beta-methoxyethyl)aminonitrobenzene

HRID 981821
Notes
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Reaction equation

HRID 981821 reaction equation
C.Cl[C:3]1[CH:8]=[C:7]([NH:9][CH2:10][CH2:11][O:12][CH3:13])[C:6]([N+:14]([O-:16])=[O:15])=[C:5]([NH:17][CH2:18][CH2:19][O:20][CH3:21])[CH:4]=1.C(O)=O>C(N(CC)CC)C.O.[Pd]>[CH3:21][O:20][CH2:19][CH2:18][NH:17][C:5]1[CH:4]=[CH:3][CH:8]=[C:7]([NH:9][CH2:10][CH2:11][O:12][CH3:13])[C:6]=1[N+:14]([O-:16])=[O:15]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 3

HCID 284Formic AcidHCID 297MethaneHCID 200710824-Chloro-2-(beta-methoxyethyl)amino-6-(beta-methoxyethyl)aminonitrobenzene

Product 1

HCID 200710692-(beta-Methoxyethyl)amino-6-(beta-methoxyethyl)aminonitrobenzene

Reagents, catalysts & solvents 3

HCID 23938PalladiumCatalyst
HCID 962
Water
Solvent
HCID 8471TriethylamineSolvent

Procedure

0.4 g of palladium at a concentration of 10% on active charcoal is added to 0.084 mole (25.5 g) of 4-chloro-2-(β-methoxyethyl)amino-6-(β-methoxyethyl)aminonitrobenzene in 33.4 ml of triethylamine, after which 7 ml of formic acid are added dropwise. At the end of the additions, the reaction mixture is heated for 1 hour 30 minutes, under reflux. The reaction mixture is diluted with 100 ml of 96° alcohol and 100 ml of water. The expected product precipitates. After filtration, the expected product containing the catalyst is dissolved in 90 ml of isopropyl alcohol. The catalyst is removed by hot filtration. The expected product crystallizes.

Workup

  1. temperatureAt the end of the additions, the reaction mixture is heated for 1 hour 30 minutes
  2. temperatureunder reflux
  3. customThe expected product precipitates
  4. filtrationAfter filtration
  5. additionthe expected product containing the catalyst
  6. dissolutionis dissolved in 90 ml of isopropyl alcohol
  7. customThe catalyst is removed by hot filtration
  8. customThe expected product crystallizes

Sources & evidence

ORD record
ord-abb8d79a029b42918187e3d6971550f6
Source dataset
uspto-grants-1991_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04992586

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes