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

HRID 1368824
ノート
印刷プレビュー

反応式

HRID 1368824 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

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 at room temperature for 30 minutes. 11.0 g (0.087 mol) of dimethyl sulfate were then added, the mixture was stirred for 12 hours at room temperature, and a further 11.0 g of dimethyl sulfate were added. The reaction mixture was heated to 60° C. for 6 hours, cooled and stirred into 2 l of ice-water. The aqueous phase was then extracted with ethyl acetate, the combined organic phases were dried and the solvent was distilled off under reduced pressure. Silica gel chromatography of the residue (eluent:toluene/ethyl acetate=9/1) afforded 2.0 g of methyl 2,4-dichloro-3-(1′-methoxyimino-1-(methoxy)methyl)benzoate.

後処理

  1. stirringthe mixture was stirred for 12 hours at room temperature
  2. temperatureThe reaction mixture was heated to 60° C. for 6 hours
  3. temperaturecooled
  4. extractionThe aqueous phase was then extracted with ethyl acetate
  5. customthe combined organic phases were dried
  6. distillationthe solvent was distilled off under reduced pressure

出典と根拠

ORDレコード
ord-87915b23253642c3a5d2cbbef555bccd
出典データセット
uspto-grants-2003_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06576596B1

反応ノート

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