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Hydrogen Peroxide → 4-Chloro-3-ethylsulfinyl-2-methylbenzoic acid

HRID 1640388
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HRID 1640388 반응식
[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[C:4]([CH3:11])[C:3]=1[S:12][CH2:13][CH3:14].[OH:15]O>C(O)(=O)C>[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[C:4]([CH3:11])[C:3]=1[S:12]([CH2:13][CH3:14])=[O:15]
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참가 물질

4

반응물 2

HCID 784Hydrogen PeroxideHCID 667391774-Chloro-3-ethylthio-2-methylbenzoic acid

생성물 1

HCID 667389094-Chloro-3-ethylsulfinyl-2-methylbenzoic acid수율 100.9%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

1.15 g (4.98 mmol) of 4-chloro-3-ethylthio-2-methylbenzoic acid in 10 ml of glacial acetic acid were heated to a temperature of 50° C.-60° C. At this temperature, 484 mg (35% strength, 4.98 mmol) of an aqueous hydrogen peroxide solution were added dropwise. The mixture was stirred at this temperature for 5 h. The reaction mixture was cooled, washed with an aqueous saturated sodium bisulfite solution and, after analytical proof of absence of peroxides, freed from the solvents. Water was added to the residue, and the mixture was acidified with 6M HCl. The mixture was extracted with ethyl acetate, and the combined organic phases were dried, filtered and, under reduced pressure, freed from the solvent. 1.24 g of the product (purify about 95% by weight) were isolated.

후처리

  1. temperatureThe reaction mixture was cooled
  2. washwashed with an aqueous saturated sodium bisulfite solution
  3. additionWater was added to the residue
  4. extractionThe mixture was extracted with ethyl acetate
  5. customthe combined organic phases were dried
  6. filtrationfiltered and, under reduced pressure

출처 및 근거

ORD 기록
ord-54ba2a81939e4b30b34714f49dc50007
출처 데이터셋
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08114816B2

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