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Hydrogen Peroxide → HCID 59578505、化合物

HRID 1774566
ノート
印刷プレビュー

反応式

HRID 1774566 の反応式
[Cl:1][C:2]1[C:7]([OH:8])=[C:6]([CH2:9][CH:10]=[CH2:11])[C:5]([CH3:12])=[CH:4][CH:3]=1.[OH-:13].[Na+].OO>O1CCCC1>[Cl:1][C:2]1[C:7]([OH:8])=[C:6]([CH2:9][CH2:10][CH2:11][OH:13])[C:5]([CH3:12])=[CH:4][CH:3]=1
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 784Hydrogen PeroxideHCID 14798Sodium HydroxideHCID 533059432-Allyl-6-chloro-3-methylphenol

生成物 1

HCID 59578505HCID 59578505、化合物収率 70%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

Under nitrogen atmosphere, a solution of 6-chloro-3-methyl-2-(prop-2-en-1-yl)phenol (7b) (8.70 g, 47.6 mmol) in anhydrous tetrahydrofuran (300 mL) was cooled to 0° C. Borane-tetrahydrofuran complex, 1.0M solution in tetrahydrofuran (100 mL, 0.10 mol) was dropwise added. The reaction mixture was stirred at room temperature for 2 hours then cooled again to 0° C. A 10N sodium hydroxide solution (32.7 mL) was added dropwise, followed by a 30% hydrogen peroxide solution. The resulting mixture was warm to room temperature and stirred for 90 minutes. The reaction mixture was quenched with a 10% hydrochloric acid solution (163 mL). Layers were separated and the aqueous layer was extract with ethyl acetate (2×70 mL). The combined organics layers were washed with brine (3×100 mL) then cooled with an ice bath. A saturated solution of sodium sulfite (150 mL) was carefully added and the mixture was stirred for few minutes. The organic layer was separated, dried over sodium sulfate and concentrated in vacuo. The residue was purified by flash chromatography on silica gel (cyclohexane/ethyl acetate 100/0 to 75/25), to provide 6-chloro-2-(3-hydroxypropyl)-3-methylphenol (7c) (6.74 g, 33.6 mmol, 70%).

後処理

  1. temperaturethen cooled again to 0° C
  2. temperatureThe resulting mixture was warm to room temperature
  3. stirringstirred for 90 minutes
  4. customThe reaction mixture was quenched with a 10% hydrochloric acid solution (163 mL)
  5. customLayers were separated
  6. extractionthe aqueous layer was extract with ethyl acetate (2×70 mL)
  7. washThe combined organics layers were washed with brine (3×100 mL)
  8. temperaturethen cooled with an ice bath
  9. additionA saturated solution of sodium sulfite (150 mL) was carefully added
  10. stirringthe mixture was stirred for few minutes
  11. customThe organic layer was separated
  12. dry with materialdried over sodium sulfate
  13. concentrationconcentrated in vacuo
  14. customThe residue was purified by flash chromatography on silica gel (cyclohexane/ethyl acetate 100/0 to 75/25)

出典と根拠

ORDレコード
ord-af6fd4d3bfb04ce6a37fb205a2c51ea9
出典データセット
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09260395B2

反応ノート

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