Water → Ethyl 4-chloro-2-(ethoxyimino)-3-oxobutanoate

HRID 2295536Notes

Reaction equation

HRID 2295536 reaction equation
S(Cl)([Cl:4])(=O)=O.[CH2:6]([O:8][N:9]=[C:10]([C:16](=[O:18])[CH3:17])[C:11]([O:13][CH2:14][CH3:15])=[O:12])[CH3:7].O>C(O)(=O)C>[CH2:6]([O:8][N:9]=[C:10]([C:16](=[O:18])[CH2:17][Cl:4])[C:11]([O:13][CH2:14][CH3:15])=[O:12])[CH3:7]

Participants

5

Reactant 3

HCID 962WaterHCID 24648Sulfuryl chlorideHCID 54511140Ethyl 2-ethoxyimino-3-oxobutyrate

Product 1

HCID 53877278Ethyl 4-chloro-2-(ethoxyimino)-3-oxobutanoateYield 93.1%

Reagents, catalysts & solvents 1

HCID 176Acetic AcidSolvent

Procedure

Sulfuryl chloride (35.2 g.) was added all at once to the stirred solution of ethyl 2-ethoxyimino-3-oxobutyrate (syn isomer, 48.9 g.) in acetic acid (49 ml.) at room temperature, and stirred at the same temperature for an hour. After adding the resultant solution into water (200 ml.), the solution was extracted with methylene chloride. The extract was washed with a saturated aqueous solution of sodium chloride, neutralized with an aqueous solution of sodium bicarbonate and washed with water. The solution was dried over magnesium sulfate and concentrated under reduced pressure to give ethyl 2-ethoxyimino-3-oxo-4-chlorobutyrate (syn isomer, 53.8 g.), pale yellow oil.

Workup

  1. extractionthe solution was extracted with methylene chloride
  2. washThe extract was washed with a saturated aqueous solution of sodium chloride
  3. washwashed with water
  4. dry with materialThe solution was dried over magnesium sulfate
  5. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-b7cf35d25a2846a8a1e80ce31817409c
Source dataset
uspto-grants-1984_01
Patent number
US04425341

Reaction notes

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