Acetic Acid → 2-(gamma-Hydroxypropyl)amino-6-(gamma-hydroxypropyl)aminonitrobenzene
Reaction equation
Cl[C:2]1[CH:7]=[C:6]([NH:8][CH2:9][CH2:10][CH2:11][OH:12])[C:5]([N+:13]([O-:15])=[O:14])=[C:4]([NH:16][CH2:17][CH2:18][CH2:19][OH:20])[CH:3]=1.C(O)(=O)C.C(O)=O.O>C(N(CC)CC)C.[Pd]>[OH:20][CH2:19][CH2:18][CH2:17][NH:16][C:4]1[CH:3]=[CH:2][CH:7]=[C:6]([NH:8][CH2:9][CH2:10][CH2:11][OH:12])[C:5]=1[N+:13]([O-:15])=[O:14]Participants
7
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
340 mg of palladium at a concentration of 10% on calcium carbonate are added to 0.017 mole (5.2 g) of 4-chloro-2-(γ-hydroxypropyl)amino-6-(γ-hydroxypropyl)amino-nitrobenzene in 11.7 ml of triethylamine. 0.9 ml of acetic acid and 2.3 ml of formic acid are then run in dropwise. A high exothermicity is noted. The reaction mixture is heated under reflux for 3 hours. 10 ml of water are added. The reaction mixture diluted in this manner is filtered hot to remove the catalyst. The expected product precipitates from the filtrate as it cools. It is filtered off, washed with water and then dried under vacuum in the presence of phosphorus pentoxide. Recrystallized from ethyl acetate, it melts at 90° C.
Workup
- temperatureThe reaction mixture is heated
- temperatureunder reflux for 3 hours
- additionThe reaction mixture diluted in this manner
- filtrationis filtered hot
- customto remove the catalyst
- customThe expected product precipitates from the filtrate as it
- filtrationIt is filtered off
- washwashed with water
- dry with materialdried under vacuum in the presence of phosphorus pentoxide
- customRecrystallized from ethyl acetate, it melts at 90° C.
Sources & evidence
- ORD record
- ord-de230ff7b8544dcb864075e32f0e1df5
- Source dataset
- uspto-grants-1991_02
- Patent number
- US04992586
Reaction notes
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