3-(3-Hydroxy-4-methoxyphenyl)prop-2-enal → 3-(3-Hydroxy-4-methoxyphenyl)propanal

HRID 1007623

反応式

HRID 1007623 の反応式
[OH:1][C:2]1[CH:3]=[C:4]([CH:9]=[CH:10][C:11]=1[O:12][CH3:13])[CH:5]=[CH:6][CH:7]=[O:8]>CO>[OH:1][C:2]1[CH:3]=[C:4]([CH2:5][CH2:6][CH:7]=[O:8])[CH:9]=[CH:10][C:11]=1[O:12][CH3:13]

参加物

3

反応条件

温度
35 °C

実験手順

3-Hydroxy-4-methoxycinnamaldehyde (8.66 g, 48.6 mmol) and 5% palladium-alumina (aluminum oxide) (0.540 g) were added to methanol (144 ml), and the mixture was stirred under hydrogen atmosphere of normal pressure (0.1 MPa) at 35° C. for 7 hours for reaction. The reaction solution was filtrated to remove the catalyst, and further the catalyst was washed with methanol (40 ml). The filtrate and the wash solution were combined together, and then concentrated. Thus concentrated solution was subjected to a purification process with a silica gel column chromatography (eluting solvent: toluene/ethyl acetate=4/1). The thus eluted fractions containing the object compound were concentrated under reduced pressure to obtain crude 3-(3-hydroxy-4-methoxyphenyl) propionaldehyde (6.86 g, 38.1 mmol, yield: 78%) in the slightly yellow coloured solid.

後処理

  1. filtrationThe reaction solution was filtrated
  2. customto remove the catalyst
  3. washfurther the catalyst was washed with methanol (40 ml)
  4. concentrationconcentrated
  5. washThus concentrated solution was subjected to a purification process with a silica gel column chromatography (eluting solvent: toluene/ethyl acetate=4/1)
  6. additionThe thus eluted fractions containing the object compound
  7. concentrationwere concentrated under reduced pressure

出典と根拠

ORDレコード
ord-809860abc8e24cb6b86d9c695f4bcadc
出典データセット
uspto-grants-2004_09
特許番号
US06794531B2

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