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Acetone → Methyl(4-chloro-3-methoxyphenyl)acetate

HRID 1686381
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HRID 1686381 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8]C(O)=O)=[CH:4][C:3]=1[OH:12].S([O:18][CH3:19])(OC)(=O)=O.[C:20](=[O:23])([O-])[O-].[K+].[K+].[CH3:26]C(C)=O>O>[CH3:20][O:23][C:19](=[O:18])[CH2:8][C:5]1[CH:6]=[CH:7][C:2]([Cl:1])=[C:3]([O:12][CH3:26])[CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 180AcetoneHCID 6497Dimethyl SulfateHCID 11430Potassium CarbonateHCID 30171834-Chloro-3-hydroxyphenylacetic acid

생성물 1

HCID 57609448Methyl(4-chloro-3-methoxyphenyl)acetate

시약·촉매·용매 1

HCID 962Water용매

실험 절차

The product of example 1 step (iii) (1 g), dimethyl sulfate (1 ml), potassium carbonate (1.48 g) and acetone (20 ml) were charged to a flask and heated at reflux for 16 h. The reaction was diluted with water, extracted with EtOAc, dried (MgSO4) and evaporated under reduced pressure to give the subtitle compound (1.5 g).

후처리

  1. temperatureheated
  2. temperatureat reflux for 16 h
  3. extractionextracted with EtOAc
  4. dry with materialdried (MgSO4)
  5. customevaporated under reduced pressure

출처 및 근거

ORD 기록
ord-79a0e8db07cf4083a40355f7741959dd
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08148572B2

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