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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Lead tetraacetate → p-Methoxyphenylpropionic acid

HRID 28762
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HRID 28762 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9](=O)[CH2:10]C)=[CH:5][CH:4]=1.C[C:14]([O-:16])=[O:15].CC([O-])=O.CC([O-])=O.CC([O-])=O.[Pb+2].C(OC(OCC)OCC)C.Cl(O)(=O)(=O)=O>[OH-].[K+].O.CO>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([CH:9]([CH3:10])[C:14]([OH:16])=[O:15])=[CH:7][CH:8]=1
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참가 물질

8

반응물 4

HCID 11025Lead tetraacetateHCID 24247Perchloric AcidHCID 31214Ethyl orthoformateHCID 671444-Propanoylanisole

생성물 1

HCID 257576p-Methoxyphenylpropionic acid수율 63.5%

시약·촉매·용매 3

HCID 887Methanol용매2회
HCID 962
Water
용매
HCID 14797Potassium Hydroxide용매

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온도
55 °C

실험 절차

A mixture of p-methoxypropiophenone (2.39 g, 14.5 mmol), 90% lead(IV)acetate (6.45 g, 14.5 mmol), triethylorthoformate (15 ml) and 70% perchloric acid (1.2 ml. 29 mmol) was heated to 55° C. for 18 h. The mixture was cooled and the triethylorthoformate removed under reduced pressure. The residue was dissolved in CHCl3 and the remaining precipitate filtered off and discarded. The CHCl3 solution was then washed with water and evaporated to yield the crude ester. This crude ester product was dissolved in a 10% KOH 1:1 water:methanol solution, which was then refluxed for 3 h. After cooling the methanol was evaporated under reduced pressure and the aqueous solution washed with diethylether (3×25 ml). The aqueous solution was acidified with 2N H2SO4, then washed again with diethylether (3×25 ml). The combined fractions from the second ether wash were dried (Na2SO4) and evaporated to give the propionic acid (1.66 g, 63%).

후처리

  1. temperatureThe mixture was cooled
  2. customthe triethylorthoformate removed under reduced pressure
  3. dissolutionThe residue was dissolved in CHCl3
  4. filtrationthe remaining precipitate filtered off
  5. washThe CHCl3 solution was then washed with water
  6. customevaporated
  7. customto yield the crude ester
  8. customwas evaporated under reduced pressure
  9. washthe aqueous solution washed with diethylether (3×25 ml)
  10. washwashed again with diethylether (3×25 ml)
  11. washThe combined fractions from the second ether wash
  12. dry with materialwere dried (Na2SO4)
  13. customevaporated

출처 및 근거

ORD 기록
ord-296cb2a7bea74433a90a47142849b1ea
출처 데이터셋
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07419998B2

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