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Lead tetraacetate → p-Methoxyphenylpropionic acid

HRID 606530
ノート
印刷プレビュー

反応式

HRID 606530 の反応式
[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
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

8

反応物 4

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

生成物 1

HCID 257576p-Methoxyphenylpropionic acid収率 63.5%

試薬・触媒・溶媒 3

HCID 887Methanol溶媒2 回
HCID 962
Water
溶媒
HCID 14797Potassium Hydroxide溶媒

反応条件

温度
55 °C

実験手順

A mixture of p-methoxypropiophenone (2.39 g, 14.5 mmol), 90%/0 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%).

後処理

  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

出典と根拠

ORDレコード
ord-d7123578424948919c7d82690b22f85c
出典データセット
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07915308B2

反応ノート

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