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3-(4-Hydroxyphenyl)propanal → 3-(4-Hydroxyphenyl)propionic acid

HRID 2415429
ノート
印刷プレビュー

反応式

HRID 2415429 の反応式
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][CH:10]=[O:11])=[CH:4][CH:3]=1.CC(C)=[O:14].OS(O)(=O)=O.O=[Cr](=O)=O>CC(C)=O>[OH:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][CH2:9][C:10]([OH:14])=[O:11])=[CH:6][CH:7]=1
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 2

HCID 119574273-(4-Hydroxyphenyl)propanalHCID 131709961Jones' reagent

生成物 1

HCID 103943-(4-Hydroxyphenyl)propionic acid収率 63.1%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

反応条件

温度
0 °C

実験手順

0.79 g (5.19 mmoles) of 3-(4-hydroxyphenyl)-1-propanal were dissolved in acetone (20 ml) and Jones reagent (chromic anhydride in sulphuric acid) (8 ml) was added to it drop by drop until the yellow-brown colour persisted. The solution was stirred for one hour at 0° C. The excess reagent was destroyed with methanol and the solution was filtered and evaporated at reduced pressure. The residue was extracted in ethyl acetate, dried over anhydrous sodium sulphate and concentrated, diving an impure residue (0.6470 g), which was chromatographed over silica gel, obtaining 0.545 g (63.1% yield) of 3-(4-hydroxyphenyl) propionic acid. Recrystallisation in methanol gave m.p.=121° C.

後処理

  1. customThe excess reagent was destroyed with methanol
  2. filtrationthe solution was filtered
  3. customevaporated at reduced pressure
  4. extractionThe residue was extracted in ethyl acetate
  5. dry with materialdried over anhydrous sodium sulphate
  6. concentrationconcentrated
  7. customdiving an impure residue (0.6470 g), which was chromatographed over silica gel

出典と根拠

ORDレコード
ord-92d91c0ded25429cb85ff1f1dc9d261b
出典データセット
uspto-grants-2004_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06818780B2

反応ノート

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