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Hexane → HCID 22169093, 화합물

HRID 566408
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HRID 566408 반응식
C[O:2][C:3](=[O:13])[C:4]1[CH:9]=[CH:8][C:7]([OH:10])=[C:6]([CH3:11])[C:5]=1[OH:12].[Cl:14]OC(C)(C)C.CCCCCC>C(OCC)(=O)C>[Cl:14][C:8]1[C:7]([OH:10])=[C:6]([CH3:11])[C:5]([OH:12])=[C:4]([CH:9]=1)[C:3]([OH:2])=[O:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8058HexaneHCID 118521Benzoic acid, 2,4-dihydroxy-3-methyl-, methyl esterHCID 521297Tert-Butyl hypochlorite

생성물 1

HCID 22169093HCID 22169093, 화합물수율 37%

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

To a solution of 2,4-dihydroxy-3-methylbenzoic acid methyl ester (9.9 g) in ethyl acetate (100 ml) was added tert-butyl hypochlorite (12.3 ml) under ice-cooling. After stirring for 2 hours, hexane (200 ml) was added, and the mixture was cooled with ice to allow precipitation of crystals. The crystals were collected by filtration, and dissolved in a mixed solvent of methanol (20 ml) and tetrahydrofuran (THF, 20 ml). A 1M lithium hydroxide solution (40 ml) was added to the solution, and the mixture was refluxed under heating for 18 hours. The reaction mixture was concentrated, and a 10% aqueous citric acid solution was added to the residue, which was followed by extraction with ethyl acetate. The organic layer was washed with water and saturated brine, and dried over anhydrous sodium sulfate. The organic layer was concentrated under reduced pressure to give the title compound (4.14 g, yield 37%).

후처리

  1. temperaturecooling
  2. temperaturethe mixture was cooled with ice
  3. customprecipitation of crystals
  4. filtrationThe crystals were collected by filtration
  5. dissolutiondissolved in a mixed solvent of methanol (20 ml) and tetrahydrofuran (THF, 20 ml)
  6. additionA 1M lithium hydroxide solution (40 ml) was added to the solution
  7. temperaturethe mixture was refluxed
  8. temperatureunder heating for 18 hours
  9. concentrationThe reaction mixture was concentrated
  10. additiona 10% aqueous citric acid solution was added to the residue, which
  11. extractionwas followed by extraction with ethyl acetate
  12. washThe organic layer was washed with water and saturated brine
  13. dry with materialdried over anhydrous sodium sulfate
  14. concentrationThe organic layer was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-92697b3fbd0041e6a4f4e17481d14e65
출처 데이터셋
uspto-grants-2001_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06174887B1

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