4-Hydroxy-3-(2-propen-1-yl)benzyl alcohol → 4-(Hydroxymethyl)-2-propylphenol
反応式
[OH:1][C:2]1[CH:9]=[CH:8][C:5]([CH2:6][OH:7])=[CH:4][C:3]=1[CH2:10][CH:11]=[CH2:12].[H][H]>C(O)C.[Rh]>[OH:1][C:2]1[CH:9]=[CH:8][C:5]([CH2:6][OH:7])=[CH:4][C:3]=1[CH2:10][CH2:11][CH3:12]参加物
5
実験手順
To a solution of 0.370 g (2.25 mmol) of the product of Step H dissolved in 25 mL of absolute ethanol was added 53 mg of a 5% rhodium on carbon catalyst and the mixture was shaken under a 40 psig pressure of hydrogen on a Parr apparatus. After 30 minutes, the reaction mixture was removed, filtered and evaporated in vacuo. The residue was purified on a silica gel flash chromatography column eluted with 35% ethyl acetate/hexane to afford the title compound.
後処理
- customthe reaction mixture was removed
- filtrationfiltered
- customevaporated in vacuo
- customThe residue was purified on a silica gel flash chromatography column
- washeluted with 35% ethyl acetate/hexane
出典と根拠
- ORDレコード
- ord-f5900e7d481242c98bc4481f29fa8eb1
- 出典データセット
- uspto-grants-1994_12
- 特許番号
- US05374638
反応ノート
読み込み中…