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

HRID 2415429
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HRID 2415429 반응식
[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
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참가 물질

4

반응물 2

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

생성물 1

HCID 103943-(4-Hydroxyphenyl)propionic acid수율 63.1%

시약·촉매·용매 1

HCID 180Acetone용매

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온도
0 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-92d91c0ded25429cb85ff1f1dc9d261b
출처 데이터셋
uspto-grants-2004_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06818780B2

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