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Tetrahydrofuran → 7,8-Dimethyl-4,4a,5,6-tetrahydro-2(3H)-naphthalenone

HRID 478071
ノート
印刷プレビュー

反応式

HRID 478071 の反応式
C([N-][CH:5]([CH3:7])[CH3:6])(C)C.[Li+].C[C:10]1[C:11](=[O:17])[CH2:12][CH2:13][CH2:14][C:15]=1[CH3:16].[CH2:18]1COC[CH2:19]1>>[CH3:18][C:19]1[CH2:16][CH2:15][CH:14]2[C:7]([C:5]=1[CH3:6])=[CH:10][C:11](=[O:17])[CH2:12][CH2:13]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 3

HCID 8028Tetrahydrofuran2 回HCID 2724682Lithium diisopropylamideHCID 108878982,3-Dimethyl-2-cyclohexen-1-one

生成物 1

HCID 124539797,8-Dimethyl-4,4a,5,6-tetrahydro-2(3H)-naphthalenone収率 60%

反応条件

温度
25 °C

実験手順

To a stirred solution of lithium diisopropylamide (LDA) (22 mmol) in THF (200 ml) at -78° C. was added a solution of 2,3-dimethylcyclohexenone (2.48 g, 20 mmol) in THF (50 ml). The mixture was warmed to 25° C., and the solvent and the amine were removed under vacuum. The resulting solid was dissolved in THF (400 ml) and the solution cooled to -78° C. To this solution was added MVK (1.8 ml, 22 mmol) in THF (100 ml) over 10 min. The resulting mixture was stirred 12 hr at room temperature, then worked up. Removal of solvent yielded the dione as a yellow oil (2.8 g, 60%).

後処理

  1. customthe solvent and the amine were removed under vacuum
  2. dissolutionThe resulting solid was dissolved in THF (400 ml)
  3. temperaturethe solution cooled to -78° C
  4. additionTo this solution was added MVK (1.8 ml, 22 mmol) in THF (100 ml) over 10 min
  5. customRemoval of solvent

出典と根拠

ORDレコード
ord-bbeec7b147a04622b97ec50f66b5c626
出典データセット
uspto-grants-1989_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04889947

反応ノート

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