Sodium Hydroxide → 2-(2-Amino-4-thiazolyl)-2-ethoxyiminoacetic acid

HRID 1659737Notes

Reaction equation

HRID 1659737 reaction equation
[CH2:1]([O:3][N:4]=[C:5]([C:11]1[N:12]=[C:13]([NH2:16])[S:14][CH:15]=1)[C:6]([O:8]CC)=[O:7])[CH3:2].[OH-].[Na+]>C(O)C>[CH2:1]([O:3][N:4]=[C:5]([C:11]1[N:12]=[C:13]([NH2:16])[S:14][CH:15]=1)[C:6]([OH:8])=[O:7])[CH3:2]

Participants

4

Procedure

Ethyl 2-ethoxyimino-2-(2-aminothiazol-4-yl)acetate (syn isomer) (5 g) was added to a mixture of 1 N sodium hydroxide (45.9 ml) and ethanol (30 ml) and stirred at room temperature for 5 hours. After removing ethanol from the resultant solution under reduced pressure, the residue was dissolved in water (60 ml) and adjusted to pH 2.0 with 10% hydrochloric acid. The solution was subjected to salting-out, and the precipitates were collected by filtration and dried to give 2-ethoxyimino-2-(2-aminothiazol-4-yl)acetic acid (syn isomer) (2.9 g).

Workup

  1. customAfter removing ethanol from the resultant solution under reduced pressure
  2. dissolutionthe residue was dissolved in water (60 ml)
  3. filtrationthe precipitates were collected by filtration
  4. customdried

Sources & evidence

ORD record
ord-179246f7d9b24c8f81e48bf97abe6709
Source dataset
uspto-grants-1981_12
Patent number
US04304770

Reaction notes

Loading…