Sodium Hydroxide → HCID 2773394, compound

HRID 1351722Notes

Reaction equation

HRID 1351722 reaction equation
[N+:1]([O-])([O-])=O.[Na+].[Br:6][C:7]1[CH:8]=[CH:9][C:10]([F:14])=[C:11]([CH:13]=1)[NH2:12].O.O.[Sn](Cl)Cl.[OH-].[Na+]>O.Cl>[Br:6][C:7]1[CH:8]=[CH:9][C:10]([F:14])=[C:11]([NH:12][NH2:1])[CH:13]=1

Participants

7

Conditions

Temperature
0 °C

Procedure

A solution of sodium nitrate (0.49 g, 0.007 mM) in water (1.5 ml) was added drop wise to a vigorously stirred heterogeneous solution of 5-bromo-2-fluoroaniline (1.4 g) in concentrated HCl(aq) (3.5 ml) over a 30 minutes period at 0° C. Tin (II) chloride dihydrate (4.5 g, 0.02 mM) in concentrated HCl(aq) (3.5 ml) was added drop wise to the above solution over a period of 30 minutes. After the addition, the solution was allowed to stir at 0° C. for one hour. The reaction solution was basified (pH>7) by slowly adding a solution of 50% aqueous NaOH to the reaction mixture. The water layer was washed with diethyl ether (3×). The organic layers were combined, dried (MgSO4), and concentrated. The resultant solid was thoroughly washed with hexanes. The undissolved solid was captured on filter and further washed with hexanes to afford 0.81 g (54% yield) of the desired product as an off-white solid. NMR (CHCl3) δ 5.45 (bs, 1H); 6.80–6.86(m, 2H); 7.25–7.28 (m, 1H).

Workup

  1. additionAfter the addition
  2. washThe water layer was washed with diethyl ether (3×)
  3. dry with materialdried (MgSO4)
  4. concentrationconcentrated
  5. washThe resultant solid was thoroughly washed with hexanes
  6. filtrationon filter
  7. washfurther washed with hexanes

Sources & evidence

ORD record
ord-250103c2717b47de8aef5528f69e92da
Source dataset
uspto-grants-2007_05
Patent number
US07217730B2

Reaction notes

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