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Dimethyl Sulfate → Ethyl 2-methoxyimino-3,3-ethylenedioxy-4-chlorobutyrate

HRID 463392
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HRID 463392 반응식
[OH:1][N:2]=[C:3]([C:9]1([O:15][CH2:14][CH2:13][O:12]1)[CH2:10][Cl:11])[C:4]([O:6][CH2:7][CH3:8])=[O:5].[C:16](=O)([O-])[O-].[K+].[K+].S(OC)(OC)(=O)=O>CC(C)=O>[CH3:16][O:1][N:2]=[C:3]([C:9]1([O:12][CH2:13][CH2:14][O:15]1)[CH2:10][Cl:11])[C:4]([O:6][CH2:7][CH3:8])=[O:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6497Dimethyl SulfateHCID 11430Potassium CarbonateHCID 86738087Ethyl 2-hydroxyimino-3,3-ethylenedioxy-4-chlorobutyrate

생성물 1

HCID 54025463Ethyl 2-methoxyimino-3,3-ethylenedioxy-4-chlorobutyrate

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

To a solution of ethyl 2-hydroxyimino-3,3-ethylenedioxy-4-chlorobutyrate (syn isomer, 0.5 g) in dried acetone (5 ml) was added potassium carbonate (0.29 g), and then dimethyl sulfate (0.265 g) was added dropwise thereto at ambient temperature with stirring. The mixture was stirred for 7 hours at ambient temperature and then filtered. The filtrate was evaporated to give ethyl 2-methoxyimino-3,3-ethylenedioxy-4-chlorobutyrate (syn isomer).

후처리

  1. stirringThe mixture was stirred for 7 hours at ambient temperature
  2. filtrationfiltered
  3. customThe filtrate was evaporated

출처 및 근거

ORD 기록
ord-9d05b9435aa442ce844054a7cee97580
출처 데이터셋
uspto-grants-1985_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04518774

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