Sodium Hydroxide → HCID 54447220, compound

HRID 1703027Notes

Reaction equation

HRID 1703027 reaction equation
[OH-].[Na+].[CH3:3][O:4][N:5]=[C:6]([C:11]1[CH:15]=[N:14][S:13][N:12]=1)[C:7]([O:9]C)=[O:8]>CO>[CH3:3][O:4][N:5]=[C:6]([C:11]1[CH:15]=[N:14][S:13][N:12]=1)[C:7]([OH:9])=[O:8]

Participants

4

Procedure

An aqueous solution of 1 N sodium hydroxide (5.4 ml.) was added with stirring at ambient temperature to a solution of methyl 2-methoxyimino-2-(1,2,5-thiadiazol-3-yl)acetate (syn isomer) (0.9 g.) in methanol (10 ml.) and the mixture was stirred for 1 hour at ambient temperature. Methanol was distilled off and water was added to the residue, after which the mixture was washed with ether. The aqueous layer was adjusted to pH 1.5 with 10% hydrochloric acid, subjected to salting-out and extracted with ether. The extract was washed with a saturated aqueous solution of sodium chloride and dried over magnesium sulfate. Ether was distilled off. Benzene was added to the residue and removed to give crystals of 2-methoxyimino-2-(1,2,5-thiadiazol-3-yl)acetic acid (syn isomer) (0.67 g.), mp 99° to 100° C.

Workup

  1. distillationMethanol was distilled off
  2. additionwater was added to the residue
  3. washafter which the mixture was washed with ether
  4. extractionextracted with ether
  5. washThe extract was washed with a saturated aqueous solution of sodium chloride
  6. dry with materialdried over magnesium sulfate
  7. distillationEther was distilled off
  8. additionBenzene was added to the residue
  9. customremoved

Sources & evidence

ORD record
ord-d8ed5e51604c4a218ef668e2755bd4d4
Source dataset
uspto-grants-1982_09
Patent number
US04350693

Reaction notes

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