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Sodium borohydride → HCID 178520751、化合物

HRID 516872
ノート
印刷プレビュー

反応式

HRID 516872 の反応式
[O:1]=[C:2]1[CH2:7][CH2:6][CH:5]([CH2:8][C:9]([O:11][CH2:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)=[O:10])[CH2:4][CH2:3]1.[BH4-].[Na+]>CO>[OH:1][C@@H:2]1[CH2:3][CH2:4][C@H:5]([CH2:8][C:9]([O:11][CH2:12][C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=2)=[O:10])[CH2:6][CH2:7]1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 4311764Sodium borohydrideHCID 58069819Benzyl 2-(4-oxocyclohexyl)acetate

生成物 1

HCID 178520751HCID 178520751、化合物収率 18%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

Benzyl 2-(4-oxocyclohexyl)acetate (5.0 g, 20.3 mmol) was dissolved in methanol (150 ml), NaBH4 (770 mg, 20.3 mmol) was added by portions to the solution at 0° C., and the mixture was stirred for 2 hr. The mixture was concentrated under reduced pressure, followed by separation with ethyl acetate and water. The organic layer was washed with saturated brine and was dried over anhydrous magnesium sulfate, and the filtrate was concentrated under reduced pressure. The residue was chromatographed on silica gel column (hexane:ethyl acetate=85:15) to give the title compound as an oil (900 mg, yield 18%).

後処理

  1. concentrationThe mixture was concentrated under reduced pressure
  2. customfollowed by separation with ethyl acetate and water
  3. washThe organic layer was washed with saturated brine
  4. dry with materialwas dried over anhydrous magnesium sulfate
  5. concentrationthe filtrate was concentrated under reduced pressure
  6. customThe residue was chromatographed on silica gel column (hexane:ethyl acetate=85:15)

出典と根拠

ORDレコード
ord-ada0855dd3a948eb81197ffce79086b2
出典データセット
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09115079B2

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート