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Aluminium lithium hydride → HCID 22504181、化合物

HRID 1814290
ノート
印刷プレビュー

反応式

HRID 1814290 の反応式
[CH3:1][C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]=1[CH2:12][C:13](=[O:15])[CH3:14].[H-].[H-].[H-].[H-].[Li+].[Al+3]>CCOCC>[CH3:1][C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]=1[CH2:12][CH:13]([OH:15])[CH3:14]
参加物反応条件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 21226445Aluminium lithium hydrideHCID 22504114HCID 22504114、化合物

生成物 1

HCID 22504181HCID 22504181、化合物

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

反応条件

温度
-78 °C

実験手順

1-(2-Methyl-naphthalen-1-yl)-propan-2-one (1.14 g, 5.76 mmol) was dissolved in Et2O (30 mL) in an argon-purged, round-bottom flask. The mixture was chilled to −78° C. and LiAlH4 (438 mg, 11.52 mmol) was added. The reaction was stirred at −78° C. for five minutes and then at room temperature for twenty minutes. TLC analysis (silica, 20% EtOAc-hexanes) indicated the reaction was complete. The reaction was chilled again to −78° C. and was carefully quenched with saturated aqueous KHSO4 (˜2 mL). The mixture was warmed to room temperature, diluted with H2O, and extracted three times with EtOAc. The organic extracts were combined, washed with brine solution, dried over Na2SO4, filtered through celite, and concentrated to give 1-(2-methyl-naphthalen-1-yl)-propan-2-ol in quantitative yield. MS (APCI) m/z 200.2 (M−H).

後処理

  1. custompurged
  2. waitat room temperature for twenty minutes
  3. temperatureThe reaction was chilled again to −78° C.
  4. customwas carefully quenched with saturated aqueous KHSO4 (˜2 mL)
  5. temperatureThe mixture was warmed to room temperature
  6. additiondiluted with H2O
  7. extractionextracted three times with EtOAc
  8. washwashed with brine solution
  9. dry with materialdried over Na2SO4
  10. filtrationfiltered through celite
  11. concentrationconcentrated

出典と根拠

ORDレコード
ord-b066ec970db140c69c3a37b0f58bbb1f
出典データセット
uspto-grants-2005_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06875765B2

反応ノート

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