Sodium Hydroxide → O-Benzylhydroxylamine

HRID 486328

Reaction equation

HRID 486328 reaction equation
[OH-].[Na+].Cl.[CH2:4]([O:11][NH2:12])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1.C(C1C(O)=CC=CN=1)=O>C(O)C.O>[CH2:4]([O:11][NH2:12])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1

Participants

5

Reactant 3

HCID 14798Sodium HydroxideHCID 102312Benzyloxyamine hydrochlorideHCID 27373323-Hydroxypicolinaldehyde

Product 1

HCID 102313O-Benzylhydroxylamine

Reagents, catalysts & solvents 1

HCID 19096565Water ethanolSolvent

Procedure

A solution of O-benzyl hydroxylamine was prepared by dissolving 2 g of sodium hydroxide (0.05 mol) and 8 g of O-benzyl hydroxylamine hydrochloride (0.05 mol) in 50 mL of 50% ethanol-water. To this solution was added 6.15 g of 2-formyl-3-hydroxypyridine (0.05 mol). The mixture was stirred for 3 h at room temperature. The precipitate was then filtered and air dried to yield 10.3 g (90.3%) of pure product; m.p. 64°-65° C. 1H NMR (CDCl3) δ: 9.72 (s, 1H, OH); 8.37 (s, 1H, CH=N); 8.13 (d of d, J=2H, J=4 Hz, 1H); 7.33 (m, 7H); 5.17 (s, 2H, CH2). Anal. Calcd. for C13H12N2O2 : C, 68.41; H, 5.30; N, 12.27. Found: C, 68.34; H, 5.32; N, 12.21.

Workup

  1. filtrationThe precipitate was then filtered
  2. customair dried

Sources & evidence

ORD record
ord-a49998643f45453da1bba60f126e5bbe
Source dataset
uspto-grants-1994_03
Patent number
US05290942

Linked notes

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