Stannous chloride dihydrate → HCID 18944276, compound
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
Reactant 3
Product 1
Reagents, catalysts & solvents 1
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 (360 MHz, D2O) δ 3.90 (2H, s, CH2); 7.06 (2H, d, J=8.7 Hz, Ar-H); 7.40 (2H, d, J=8.7 Hz, Ar-H).
Workup
- customdid not rise above -10° C
- stirringThe mixture was stirred at -10° C. for 0.25 h
- filtrationbefore being filtered rapidly under vacuum into an addition funnel
- customthe temperature below -5° C
- temperatureto warm to room temperature
- stirringstir for 0.25 h
- filtrationbefore filtering the sandy coloured precipitate under vacuum
- washwashing with ether (5×500 ml)
- dry with materialThe resultant solid was dried over P2O5 in a vacuum oven (80° C.) for 16 h
Sources & evidence
- ORD record
- ord-044b04b1068f46b08e1a8a5f08e03a7e
- Source dataset
- uspto-grants-1994_03
- Patent number
- US05298520
Reaction notes
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