Tin dichloride dihydrate → 3,6-Bis(trifluoromethyl)benzene-1,2-diamine

HRID 868966Notes

Reaction equation

HRID 868966 reaction equation
[N+:1]([C:4]1[C:9]([C:10]([F:13])([F:12])[F:11])=[CH:8][CH:7]=[C:6]([C:14]([F:17])([F:16])[F:15])[C:5]=1[NH2:18])([O-])=O.Cl[Sn]Cl.O>CO.Cl>[F:11][C:10]([F:12])([F:13])[C:9]1[CH:8]=[CH:7][C:6]([C:14]([F:17])([F:16])[F:15])=[C:5]([NH2:18])[C:4]=1[NH2:1]

Participants

5

Conditions

Temperature
50 °C

Procedure

To a solution of 2-nitro-3,6-bis(trifluoromethyl)benzenamine (2.3 g, 8.4 mmol) in methanol (10 mL) was added a solution of SnCl2.H2O (7.56 g, 33.6 mmol) in concentrated HCl (15 mL). The mixture was heated to 50° C. and stirred for 2 hours. Methanol was removed in vacuum and the aqueous solution was basified with sodium hydroxide solution. The suspension was diluted with EtOAc (150 mL), and the mixture was stirred at room temperature for 30 minutes and filtered. The filtrate was washed with brine (100 mL), dried over sodium sulfate, and filtered. The solution was concentrated to give a crude product of 3,6-bis(trifluoromethyl)benzene-1,2-diamine (1.5 g). MS (ESI): m/z 245 [M+H]+

Workup

  1. customMethanol was removed in vacuum
  2. additionThe suspension was diluted with EtOAc (150 mL)
  3. stirringthe mixture was stirred at room temperature for 30 minutes
  4. filtrationfiltered
  5. washThe filtrate was washed with brine (100 mL)
  6. dry with materialdried over sodium sulfate
  7. filtrationfiltered
  8. concentrationThe solution was concentrated

Sources & evidence

ORD record
ord-a1497c955a2142be9dea65c796d4b299
Source dataset
uspto-grants-2015_03
Patent number
US08969349B2

Reaction notes

Loading…