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Hydrochloric Acid → 4-(2-Methylphenyl)cyclohexanone

HRID 429717
ノート
印刷プレビュー

反応式

HRID 429717 の反応式
C1O[C:4]2([CH2:9][CH2:8][C:7]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=3[CH3:17])(O)[CH2:6][CH2:5]2)[O:3]C1.Cl.[H][H]>O1CCOCC1.[Pd]>[CH3:17][C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=1[CH:7]1[CH2:8][CH2:9][C:4](=[O:3])[CH2:5][CH2:6]1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 313Hydrochloric AcidHCID 544507798-(o-Tolyl)-1,4-dioxaspiro[4.5]decan-8-olHCID 178418361HCID 178418361、化合物

生成物 1

HCID 183526694-(2-Methylphenyl)cyclohexanone収率 35%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 312751,4-Dioxane溶媒

実験手順

A solution of 4-(2-methylphenyl)-4-hydroxycyclohexanone ethylene ketal from the preceding step in 800 mL dioxane was treated with 16 mL concentrated hydrochloric acid and 30 grams 10% palladium-on-carbon under 35 p.s.i. hydrogen for 24 hours, then filtered through Celite to remove the catalyst. The filtrate was treated with 230 mL water and stirred at room temperature for 48 hours. The solution was evaporated, the pH adjusted to 8 with saturated aqueous sodium bicarbonate solution, and extracted with methylene chloride. The organic layer was dried over sodium sulfate and evaporated. The residue was chromatographed on silica gel using ethyl acetate/hexanes as eluent to afford 33.3 grams (35%) of an oil.

後処理

  1. filtrationfiltered through Celite
  2. customto remove the catalyst
  3. additionThe filtrate was treated with 230 mL water
  4. customThe solution was evaporated
  5. extractionextracted with methylene chloride
  6. dry with materialThe organic layer was dried over sodium sulfate
  7. customevaporated
  8. customThe residue was chromatographed on silica gel

出典と根拠

ORDレコード
ord-90f69e579b1f4065802ba9a229f178bf
出典データセット
uspto-grants-2001_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06319915B1

反応ノート

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