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Isopropanol → 3-phenylthiophene-2-carboxylic Acid

HRID 1611601
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HRID 1611601 반응식
CC(C)=[O:3].OS(O)(=O)=O.O=[Cr](=O)=O.[C:14]1([C:20]2[CH:24]=[CH:23][S:22][C:21]=2[CH:25]=[O:26])[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.C(O)(C)C>CC(C)=O>[C:14]1([C:20]2[CH:24]=[CH:23][S:22][C:21]=2[C:25]([OH:3])=[O:26])[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 3776IsopropanolHCID 8188473-Phenyl-2-thiophenecarboxaldehydeHCID 131709961Jones' reagent

생성물 1

HCID 25176253-phenylthiophene-2-carboxylic Acid수율 46%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

8N Jones' reagent (ca. 10 ml) was added dropwise to a solution of 3-phenylthiophen-2-aldehyde (5) (0.58 g, 3.1 mmol) in 32 ml of acetone, until an orange colour persisted. The mixture was stirred at room temperature for 18 hrs. Isopropanol (5 ml) was added to remove the excess Jones' reagent and the mixture was then filtered, the organic solvents were evaporated under vacuum and extracted with ethyl acetate (4×100 ml). The combined organic layer was washed with a saturated solution of NaCl, dried (Na2SO4), and evaporated under reduced pressure. The mixture was then chromatographed using 95/5 chloroform/methanol, thus giving the compound (6) (0.44 g, 1.36 mmol, 46% yield) (M. Pt. 200–202° C.). 1H-NMR (CDCl3) ä 6.87–7.37 (m, 5H, Ph-H) 7.05 (d J=5.0 Hz, 1H, th-H4), 7.53 (d J=5.0 Hz, 1H, th-H5).

후처리

  1. customto remove the excess Jones' reagent
  2. filtrationthe mixture was then filtered
  3. customthe organic solvents were evaporated under vacuum
  4. extractionextracted with ethyl acetate (4×100 ml)
  5. washThe combined organic layer was washed with a saturated solution of NaCl
  6. dry with materialdried (Na2SO4)
  7. customevaporated under reduced pressure
  8. customThe mixture was then chromatographed

출처 및 근거

ORD 기록
ord-ba4876600699418ab19322d3af3c4d4f
출처 데이터셋
uspto-grants-2006_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06989388B2

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