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Hexane → HCID 22169093、化合物

HRID 566408
ノート
印刷プレビュー

反応式

HRID 566408 の反応式
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]
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 8058HexaneHCID 118521Benzoic acid, 2,4-dihydroxy-3-methyl-, methyl esterHCID 521297Tert-Butyl hypochlorite

生成物 1

HCID 22169093HCID 22169093、化合物収率 37%

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate溶媒

実験手順

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%).

後処理

  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

出典と根拠

ORDレコード
ord-92697b3fbd0041e6a4f4e17481d14e65
出典データセット
uspto-grants-2001_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06174887B1

反応ノート

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