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Sodium Hydroxide → Benzonorbornadienone

HRID 1534429
ノート
印刷プレビュー

反応式

HRID 1534429 の反応式
[C:1]12[CH2:7][C:4](=[CH:5][CH:6]=1)[C:3]1[CH:8]=[CH:9][CH:10]=[CH:11][C:2]2=1.[OH-:12].[Na+].[BH4-].[Na+]>O.O1CCCC1>[C:4]12[C:5](=[O:12])[CH:6]=[C:1]([CH:7]=1)[C:2]1[CH:11]=[CH:10][CH:9]=[CH:8][C:3]2=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 14798Sodium HydroxideHCID 4311764Sodium borohydrideHCID 566125711,4-Methanonaphthalene

生成物 1

HCID 129692535Benzonorbornadienone

試薬・触媒・溶媒 2

HCID 962Water溶媒2 回HCID 8028Tetrahydrofuran溶媒

実験手順

A solution of mercuric acetate (4 g) in water (10 ml) was treated with a solution of benzobicyclo[2.2.1]heptadiene (2 g) in tetrahydrofuran (25 ml) and the resulting mixture was stirred at room temperature for 24 hours. The solution was treated with a solution of 10% sodium hydroxide in water (5 ml), followed by sodium borohydride (0.5 g). The resulting mixture was stirred for 30 minutes and the resulting layers were separated. The aqueous layer was extracted with ether (2×30 ml) and the combined organic layers were dried over magnesium sulfate and concentrated on a rotary evaporator. The residue was combined with methylene chloride (25 ml) and pyridinium chlorochromate (3 g) and the solution was stirred at room temperature for 12 hours. The solution was washed with water (30 ml) and the organic layer was dried over magnesium sulfate. The solvent was removed on a rotary evaporator and the product was purified by preparative centrifugally accelerated radial thin layer chromatography using 25% ethyl acetate in hexane as the eluant. After removal of the eluant on a rotary evaporator, the product was obtained as a yellow oil.

後処理

  1. stirringThe resulting mixture was stirred for 30 minutes
  2. customthe resulting layers were separated
  3. extractionThe aqueous layer was extracted with ether (2×30 ml)
  4. dry with materialthe combined organic layers were dried over magnesium sulfate
  5. concentrationconcentrated on a rotary evaporator
  6. stirringthe solution was stirred at room temperature for 12 hours
  7. washThe solution was washed with water (30 ml)
  8. dry with materialthe organic layer was dried over magnesium sulfate
  9. customThe solvent was removed on a rotary evaporator
  10. customthe product was purified by preparative centrifugally accelerated radial thin layer chromatography
  11. customAfter removal of the eluant
  12. customon a rotary evaporator
  13. customthe product was obtained as a yellow oil

出典と根拠

ORDレコード
ord-d4ed203921c14fd6b0005de9ed37c05d
出典データセット
uspto-grants-1992_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05089506

反応ノート

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