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Chemical Structure| 7575-35-1 Chemical Structure| 7575-35-1

Structure of 7575-35-1

Chemical Structure| 7575-35-1

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Product Details of [ 7575-35-1 ]

CAS No. :7575-35-1
Formula : C10H16N2O2
M.W : 196.25
SMILES Code : NC1=CC=C(N(CCO)CCO)C=C1
English Name :2,2'-((4-Aminophenyl)azanediyl)diethanol
MDL No. :MFCD02152657

Safety of [ 7575-35-1 ]

Application In Synthesis of [ 7575-35-1 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 7575-35-1 ]

[ 7575-35-1 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 28443-52-9 ]
  • [ 7575-35-1 ]
  • [ 55302-69-7 ]
YieldReaction ConditionsOperation in experiment
(i) aq. NaOH, (ii) aq. (NH4)2S2O8; Multistep reaction;
With sodium hydroxide In ethanol
  • 2
  • [ 18226-17-0 ]
  • [ 7575-35-1 ]
YieldReaction ConditionsOperation in experiment
100% With 10% Pd/C; hydrogen In methanol at 20℃;
94% With hydrogenchloride; tin(ll) chloride In water for 1h; Heating;
92% With hydrogen In methanol for 2h; Inert atmosphere; 21.3A.2 Step: 3A-2Synthesis of 2- [(4- Amino-phenyl)-(2-hydroxy-ethyl)-amino] -ethanol.Procedure:Pd-C (150mg) was added to a solution of 2-[(2-Hydroxy-ethyl)-(4-nitro-phenyl)- amino] -ethanol (500mg, 2.21mmol) in methanol under nitrogen atmosphere and was stirred for 2hrs under hydrogen pressure. The reaction was monitored by the TLC (10% methanol: chloroform). The resulting reaction mixture was filtered through celite bed and was concentrated to afford 400mg (92% yield) of 2-[(4-Amino-phenyl)-(2-hydroxy-ethyl)- amino]-ethanol.
With hydrogen In ethanol
With 10% Pd/C; hydrogen In methanol; dichloromethane at 20℃; 1.3 The third step: synthesis of N-(4-aminophenyl)diethanolamine (Intermediate 5) Specific procedure: Intermediate 4 (1.5g) was dissolved in CH3OH/DCM (v:v, 1:2)The mixed solution was stirred under a hydrogen atmosphere, and then 10% Pd/C (0.5 g) was added.After the reaction was completed, it was filtered through celite, and the filtrate was collected.The solvent was distilled off under reduced pressure to give a brown brown intermediate 5, which was directly reacted.

  • 3
  • [ 121-18-6 ]
  • [ 7575-35-1 ]
  • [ 118266-09-4 ]
YieldReaction ConditionsOperation in experiment
With sodium carbonate; In water; 1. 2-Nitro-4'-N,N-bis(2-hydroxyethyl)-aminodiphenylamine-4-sulfonic acid, sodium salt A mixture of (A) 6.5 g (0.025 mol) <strong>[121-18-6]4-chloro-3-nitrobenzenesulfonic acid</strong>, Na salt and (B) 4.9 g (0.025 mol) N,N-bis-(2-hydroxyethyl)-p-phenylenediamine, 2.54 g (0.027 mol) sodium carbonate and 10 ml water were heated for 7 hours to 120° C. in autoclave. After cooling, the solution was concentrated to dryness. The residue was recrystallized from a mixtue of ethanol and water. Yield: red-brown crystals, TLC (silica gel 60F-254/Merck) eluent: n-butanol/acetic acid/water=8:2:1; RF=0.42.
 

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