反応式
C(C=C)=O.O1[CH2:10][CH2:9][CH2:8][CH2:7][CH2:6]1.[CH:11]1[CH:16]=[CH:15]C=[CH:13][CH:12]=1>>[CH3:6][CH:7]=[CH:8][CH2:9][CH2:10][CH2:13][CH2:12][CH2:11][CH2:16][CH3:15]参加物
4
実験手順
In this example, inverse electron demand D-A reaction of acrolein with 3,4-tetrahydropyran is described. The procedure involves refluxing of 0.056 g of acrolein, 1.68 g of tetrahydropyran and 0.30 g of the catalyst prepared according to example 1 above in 10 ml of benzene at 60 (C 20 h. The catalyst was filtered off. After evaporation of solvent, the residue was chromatographed over silica gel column by eluting with 5% acetone/petroleum ether to give 0.12 g of endo adduct, 1,9-dioxabicyclo[4.4.05,10 ]dec-2-ene
後処理
- customprepared
- customC 20 h
- filtrationThe catalyst was filtered off
- customAfter evaporation of solvent
- customthe residue was chromatographed over silica gel column
- washby eluting with 5% acetone/petroleum ether
出典と根拠
- ORDレコード
- ord-490cabac7d5e47ccaa7ee9b756644af8
- 出典データセット
- uspto-grants-1999_08
- 特許番号
- US05932752
関連ノート
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