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Acetone → p-Prenylacetophenone

HRID 1413829
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인쇄 미리보기

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HRID 1413829 반응식
[CH3:1][C:2]1([C:7]2[CH:12]=[CH:11][C:10]([CH2:13][CH:14]=[C:15]([CH3:17])[CH3:16])=[CH:9][CH:8]=2)OCC[O:3]1.Cl.CC(C)=O.C(=O)([O-])O.[Na+]>O>[CH2:13]([C:10]1[CH:9]=[CH:8][C:7]([C:2](=[O:3])[CH3:1])=[CH:12][CH:11]=1)[CH:14]=[C:15]([CH3:17])[CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 180AcetoneHCID 313Hydrochloric AcidHCID 516892Sodium BicarbonateHCID 204676122-Methyl-2-(p-prenylphenyl)-1,3-dioxolane

생성물 1

HCID 11217703p-Prenylacetophenone수율 97.6%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A solution of 69.0 g of 2-methyl-2-(p-prenylphenyl)-1,3-dioxolane, 8 ml of 6 N hydrochloric acid and 400 ml of acetone was stirred at room temperature for 3 hours. A solution of 5.0 g of sodium hydrogen carbonate and 200 ml of water was added to the solution, which was extracted with ethyl ether after removal of the acetone. The ethereal solution was washed with water, dried, concentrated and distilled to give 54.6 g of p-prenylacetophenone, b.p. 110-112 °C/0.05 mmHg.

후처리

  1. extractionwas extracted with ethyl ether
  2. customafter removal of the acetone
  3. washThe ethereal solution was washed with water
  4. customdried
  5. concentrationconcentrated
  6. distillationdistilled

출처 및 근거

ORD 기록
ord-a9fd5e64dd0b45859c5e987ee649d3af
출처 데이터셋
uspto-grants-1981_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04251543

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