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Dimethyl Sulfate → Methyl 2,4-dichloro-3-(1'-methoxyimino-1-(methoxy)methyl)benzoate

HRID 377547
Notes
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Reaction equation

HRID 377547 reaction equation
[Cl:1][C:2]1[C:11]([C:12]([NH:14][O:15][CH3:16])=[O:13])=[C:10]([Cl:17])[CH:9]=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5].[C:18](=O)([O-])[O-].[K+].[K+].S(OC)(OC)(=O)=O>CN(C)C=O>[Cl:1][C:2]1[C:11]([C:12](=[N:14][O:15][CH3:16])[O:13][CH3:18])=[C:10]([Cl:17])[CH:9]=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 6497Dimethyl Sulfate2×HCID 11430Potassium CarbonateHCID 18517407Methyl 2,4-dichloro-3-methoxyaminocarbonylbenzoate

Product 1

HCID 53659114Methyl 2,4-dichloro-3-(1'-methoxyimino-1-(methoxy)methyl)benzoateYield 11.8%

Reagents, catalysts & solvents 1

HCID 6228Dimethylformamide
Solvent

Procedure

A mixture of 16.0 g (0.058 mol) of methyl 2,4-dichloro-3-methoxyaminocarbonylbenzoate and 10.1 g (0.073 mol) of potassium carbonate in 300 ml of dimethylformamide was stirred for 30 minutes at room temperature. 11.0 g (0.087 mol) of dimethyl sulfate were subsequently added dropwise, the mixture was stirred for 12 hours at room temperature, and another 11.0 g of dimethyl sulfate were added. After the mixture had been heated for 6 hours at 60° C., it was cooled and stirred into 2 l of ice-water. Then, the aqueous phase was extracted with ethyl acetate, the combined organic phases were dried and the solvent was distilled off in vacuo. After chromatography of the residue on silica gel (eluant:toluene/ethyl acetate=9/1), 2.0 g of methyl 2,4-dichloro-3-(1'-methoxyimino-1'-(methoxy)methyl)benzoate were obtained.

Workup

  1. stirringthe mixture was stirred for 12 hours at room temperature
  2. temperatureAfter the mixture had been heated for 6 hours at 60° C.
  3. temperatureit was cooled
  4. extractionThen, the aqueous phase was extracted with ethyl acetate
  5. customthe combined organic phases were dried
  6. distillationthe solvent was distilled off in vacuo

Sources & evidence

ORD record
ord-66b20f9e23c14cd8844274d71612d04f
Source dataset
uspto-grants-2000_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06028035

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes