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1,5-Dimethyl-8-oxabicyclo[3.2.1]oct-6-en-3-one → HCID 13534071、化合物

HRID 1583860
ノート
印刷プレビュー

反応式

HRID 1583860 の反応式
[H-].[Al+3].[Li+].[H-].[H-].[H-].[CH3:7][C:8]12[O:15][C:12]([CH3:16])([CH:13]=[CH:14]1)[CH2:11][C:10](=[O:17])[CH2:9]2>C(OCC)C>[CH3:16][C:12]12[O:15][C:8]([CH3:7])([CH:14]=[CH:13]1)[CH2:9][CH:10]([OH:17])[CH2:11]2
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 135340701,5-Dimethyl-8-oxabicyclo[3.2.1]oct-6-en-3-oneHCID 21226445Aluminium lithium hydride

生成物 1

HCID 13534071HCID 13534071、化合物収率 128.3%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒2 回

反応条件

温度
0 °C

実験手順

To a stirred suspension of lithium aluminum hydride (4.6 g of a 57% oil suspension) in dry diethyl ether (300 ml) was added a solution of 1,5-dimethyl-8-oxabicyclo[3.2.1]oct-6-en-3-one (10.0 g) in diethyl ether (50 ml) over 0.5 hour at 20° C. The reaction mixture was held for 2 hours at 20° C., cooled to 0° C., and washed successively with water (2.5 ml), 15% aqueous sodium hydroxide (2.5 ml) and water (7.5 ml), and filtered. The filter cake was washed with diethyl ether, and the combined ether filtrates were dried (MgSO4), filtered and concentrated to give 13.0 g of oil. The oil was eluted through a column of florisil first with hexane and then diethyl ether. The ether fractions were combined and concentrated to give the desired product (10.0 g) as a 66:34 mixture of epimers.

後処理

  1. washwashed successively with water (2.5 ml), 15% aqueous sodium hydroxide (2.5 ml) and water (7.5 ml)
  2. filtrationfiltered
  3. washThe filter cake was washed with diethyl ether
  4. dry with materialthe combined ether filtrates were dried (MgSO4)
  5. filtrationfiltered
  6. concentrationconcentrated

出典と根拠

ORDレコード
ord-11d08819028b468e9372e7f0eae8a6f7
出典データセット
uspto-grants-1985_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04554366

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート