反応式
[CH:1](=[O:9])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[CH2:10]=O>>[CH2:3]([C:2](=[CH2:10])[CH:1]=[O:9])[CH2:4][CH2:5][CH2:6][CH2:7][CH3:8]参加物
3
実験手順
100 G (0.78 mmol) of n-octanal, 73 g of 36% formic aldehyde and 260 g (0.78 mol) of catalyst (aqueous diethylamine chlorhydrate; 3 mol/kg) were charged in a 3-neck flask. The mixture was heated to reflux for 1 h and distilled. The reaction product was extracted with ether, dried and concentrated to give 42.41 g of 2-hexyl-2-propenal. Extraction of the flask's residue provided yet 64 g of raw product. The aldehyde was used as such in the next step.
後処理
- temperatureThe mixture was heated
- temperatureto reflux for 1 h
- distillationdistilled
- extractionThe reaction product was extracted with ether
- customdried
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-9554cf61c99e458f83aa67612c5cd11c
- 出典データセット
- uspto-grants-1994_03
- 特許番号
- US05298486
関連ノート
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