Hydrochloric Acid → HCID 22675496, compound

HRID 1106813Notes

Reaction equation

HRID 1106813 reaction equation
[CH2:1]([NH:3][CH2:4][C:5]1[CH:10]=[C:9]([Br:11])[CH:8]=[CH:7][C:6]=1[N+:12]([O-])=O)[CH3:2].Cl>C(O)C>[CH2:1]([NH:3][CH2:4][C:5]1[CH:10]=[C:9]([Br:11])[CH:8]=[CH:7][C:6]=1[NH2:12])[CH3:2]

Participants

4

Procedure

Stannous chloride dihydrate (22.5 g, 0.1 M) was added in one portion to a stirred mixture of N-ethyl-5-bromo-2-nitrobenzylamine (8.5 g, 32.8 mmol) and 36% hydrochloric acid (20 ml, 0.22M) in ethanol (250 ml) at ambient temperature. There was an exothermic reaction (50° C.) and a yellow solution formed, which was stirred for 1 hour allowing it to cool. The solvent was evaporated at reduced pressure and the residue dissolved in ethanol (100 ml) and stirred while diluting with ether (200 ml) until crystallisation occurred. The yellow solid was filtered off and washed with ether to give N-ethyl-5-bromo-2-aminobenzylamine as a salt, from which the free base was isolated by stirring with 2N sodium hydroxide solution (150 ml) and extracting into ether. The organic layer was dried over anhydrous magnesium sulphate and evaporated to give an oil (4.2 g).

Workup

  1. customan exothermic reaction (50° C.)
  2. customa yellow solution formed
  3. temperatureto cool
  4. customThe solvent was evaporated at reduced pressure
  5. dissolutionthe residue dissolved in ethanol (100 ml)
  6. stirringstirred
  7. additionwhile diluting with ether (200 ml) until crystallisation
  8. filtrationThe yellow solid was filtered off
  9. washwashed with ether

Sources & evidence

ORD record
ord-b6469a290ab740ffbdc591b33d71b89a
Source dataset
uspto-grants-2000_05
Patent number
US06057345

Reaction notes

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