Ethyl 4-bromo-3-oxobutanoate → HCID 178472904, compound

HRID 261671

Reaction equation

HRID 261671 reaction equation
[N:1]([O-:3])=O.[Na+].[Br:5][CH2:6][C:7](=[O:14])[CH2:8][C:9]([O:11][CH2:12][CH3:13])=[O:10]>O.C(O)(=O)C>[OH:3][N:1]=[C:8]([C:7]([CH2:6][Br:5])=[O:14])[C:9]([O:11][CH2:12][CH3:13])=[O:10]

Participants

5

Conditions

Temperature
10 °C

Procedure

A solution of sodium nitrite (12.4 g.) in water (150 ml.) was dropwise added with stirring at 5° to 7° C. to a solution of ethyl 4-bromoacetoacetate (30 g.) in acetic acid (200 ml.) and the mixture was stirred for 2 hours at 10° C. Water (200 ml.) was added to the reaction mixture and the resultant mixture was extracted with ether (500 ml.). The extract was washed twice with water (200 ml.) and with a sodium chloride aqueous solution (200 ml.) and dried over magnesium sulfate. The solvent was distilled off under reduced pressure to give yellowish brown crystals of ethyl 2-hydroxyimino-4-bromoacetoacetate (a mixture of syn and anti isomers) (32.6 g.).

Workup

  1. extractionthe resultant mixture was extracted with ether (500 ml.)
  2. washThe extract was washed twice with water (200 ml.) and with a sodium chloride aqueous solution (200 ml.)
  3. dry with materialdried over magnesium sulfate
  4. distillationThe solvent was distilled off under reduced pressure

Sources & evidence

ORD record
ord-d45a7d3ae8ca443dbb7fd8db381bb342
Source dataset
uspto-grants-1979_08
Patent number
US04166115

Linked notes

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