O-Methylhydroxylamine hydrochloride → HCID 178502897, compound

HRID 1584029Notes

Reaction equation

HRID 1584029 reaction equation
[SH:1][C:2]1[N:6]([CH2:7][C:8]([OH:10])=O)[N:5]=[N:4][N:3]=1.Cl.[CH3:12][O:13][NH2:14].CO.C[O-].[Na+]>CN(C)C=O>[CH3:12][O:13][NH:14][C:8](=[O:10])[CH2:7][N:6]1[C:2]([SH:1])=[N:3][N:4]=[N:5]1

Participants

5

Conditions

Temperature
0 °C

Procedure

To an ice cold and stirred solution of 5-mercapto-1H-tetrazole-1-acetic acid (9.6 g) in N,N-dimethylformamide (60 ml) is added N,N'-carbonyldiimidazole (11.6 g), and the mixture is stirred at 0° C. for 1 hour. To this mixture is added a solution of methoxyamine hydrochloride (11.6 g) in a mixture of N,N-dimethylformamide (45 ml) and 4.6 N-sodium methoxide methanol solution (28.5 ml) and the whole mixture is stirred under ice cooling for 1 hour. The reaction mixture is poured onto ice water and extracted with a mixture of ethyl acetate and methyl ethyl ketone (2:1). The extract solution is washed with water, dried and concentrated in vacuum. The residue is crystallized from a mixture of acetone and ether to give 5-mercapto-1H-tetrazole-1-acetohydroxamic acid methyl ester (7.73 g). mp. 175°-176° C. (decomp.).

Workup

  1. stirringthe whole mixture is stirred under ice cooling for 1 hour
  2. additionThe reaction mixture is poured onto ice water
  3. extractionextracted with a mixture of ethyl acetate and methyl ethyl ketone (2:1)
  4. washThe extract solution is washed with water
  5. customdried
  6. concentrationconcentrated in vacuum
  7. customThe residue is crystallized from a mixture of acetone and ether

Sources & evidence

ORD record
ord-caac92445b0f4e8eb43089910212597a
Source dataset
uspto-grants-1985_11
Patent number
US04555578

Reaction notes

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