Hydroxyamine hydrochloride → N-hydroxy-2-[[4-methoxybenzenesulfonyl](benzyl)amino]propionamide

HRID 264291Notes

Reaction equation

HRID 264291 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([S:9]([N:12]([CH2:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[CH:13]([CH3:18])[C:14](OC)=[O:15])(=[O:11])=[O:10])=[CH:5][CH:4]=1.Cl.[NH2:27][OH:28].C[O-].[Na+]>CO>[OH:28][NH:27][C:14](=[O:15])[CH:13]([N:12]([S:9]([C:6]1[CH:7]=[CH:8][C:3]([O:2][CH3:1])=[CH:4][CH:5]=1)(=[O:11])=[O:10])[CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)[CH3:18]

Participants

5

Reactant 3

HCID 443297Hydroxyamine hydrochlorideHCID 10942334Sodium MethoxideHCID 22907154Methyl 2-[[4-methoxybenzenesulfonyl](benzyl)amino]propionate

Product 1

HCID 15296597N-hydroxy-2-[[4-methoxybenzenesulfonyl](benzyl)amino]propionamide

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

(a) Methyl 2-[[4-methoxybenzenesulfonyl](benzyl)amino]propionate (2.1 g, 6.01 mmol) is dissolved in methanol (20.0 mL). To this solution is added hydroxylamine hydrochloride (0.84 g, 12.0 mmol), followed by the addition of sodium methoxide (7.0 mL of a 4.37M solution). The reaction is stirred overnight at room temperature. The reaction is worked up by first removing all the solvent, and partitioning between ethyl acetate/hexane (2/1) and saturated sodium bicarbonate. The aqueous phase is extracted well with ethyl acetate/hexane, the combined organic layers are dried (MgSO4), and the solvent is evaporated. The product is purified by silica gel chromatography (ethyl acetate) to give N-hydroxy-2-[[4-methoxybenzenesulfonyl](benzyl)amino]propionamide, m.p. 149°-151° C.

Workup

  1. customby first removing all the solvent
  2. custompartitioning between ethyl acetate/hexane (2/1) and saturated sodium bicarbonate
  3. extractionThe aqueous phase is extracted well with ethyl acetate/hexane
  4. dry with materialthe combined organic layers are dried (MgSO4)
  5. customthe solvent is evaporated
  6. customThe product is purified by silica gel chromatography (ethyl acetate)

Sources & evidence

ORD record
ord-128d36b7734c46b788bba0eff1f36ce6
Source dataset
uspto-grants-1997_07
Patent number
US05646167

Reaction notes

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