Stannous chloride dihydrate → HCID 18944276, compound

HRID 2399703Notes

Reaction equation

HRID 2399703 reaction equation
[N:1]([O-])=O.[Na+].[NH2:5][C:6]1[CH:14]=[CH:13][C:9]([CH2:10][C:11]#[N:12])=[CH:8][CH:7]=1.O.O.[Cl:17][Sn]Cl>Cl>[ClH:17].[NH:5]([C:6]1[CH:14]=[CH:13][C:9]([CH2:10][C:11]#[N:12])=[CH:8][CH:7]=1)[NH2:1]

Participants

5

Conditions

Temperature
-10 °C

Procedure

A solution of NaNO2 (80 g, 1.16 mol) was added dropwise to a cooled (-10° C.), stirred, suspension of 4-aminobenzyl cyanide (153.5 g, 1.16 mol) in concentrated HCl (1500 ml), at such a rate that the temperature did not rise above -10° C. The mixture was stirred at -10° C. for 0.25 h before being filtered rapidly under vacuum into an addition funnel. The solution was added portionwise over a 0.25 h period to a rapidly stirred mixture of SnCl2.2H2O (1.05 kg, 4.64 mol) in concentrated HCl (800 ml) keeping the temperature below -5° C. The mixture was allowed to warm to room temperature and stir for 0.25 h before filtering the sandy coloured precipitate under vacuum and washing with ether (5×500 ml). The resultant solid was dried over P2O5 in a vacuum oven (80° C.) for 16 h to give the title compound (213 g, 100%), m.p. 181°-183° C.; 1H NMR (360MHz, D2O) δ3.90 (2H, s, CH2); 7.06 (2H, d, J=8.7 Hz, Ar--H); 7.40 (2H, d, J=8.7 Hz, Ar--H).

Workup

  1. customdid not rise above -10° C
  2. stirringThe mixture was stirred at -10° C. for 0.25 h
  3. filtrationbefore being filtered rapidly under vacuum into an addition funnel
  4. customthe temperature below -5° C
  5. temperatureto warm to room temperature
  6. stirringstir for 0.25 h
  7. filtrationbefore filtering the sandy coloured precipitate under vacuum
  8. washwashing with ether (5×500 ml)
  9. dry with materialThe resultant solid was dried over P2O5 in a vacuum oven (80° C.) for 16 h

Sources & evidence

ORD record
ord-827ddca53ca54e7083554783bb9fdd9e
Source dataset
uspto-grants-1995_09
Patent number
US05451588

Reaction notes

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