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4-(2-Methyl-3-(4-chlorobenzoyl)phenyl)butanoic acid → HCID 21495671、化合物

HRID 1731164
ノート
印刷プレビュー

反応式

HRID 1731164 の反応式
[CH3:1][O-:2].[K+].Cl[C:5]1[CH:25]=[CH:24][C:8]([C:9]([C:11]2[C:12]([CH3:23])=[C:13]([CH2:17][CH2:18][CH2:19][C:20]([OH:22])=[O:21])[CH:14]=[CH:15][CH:16]=2)=[O:10])=[CH:7][CH:6]=1>CO>[CH3:1][O:2][C:5]1[CH:25]=[CH:24][C:8]([C:9]([C:11]2[C:12]([CH3:23])=[C:13]([CH2:17][CH2:18][CH2:19][C:20]([OH:22])=[O:21])[CH:14]=[CH:15][CH:16]=2)=[O:10])=[CH:7][CH:6]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 1910664-(2-Methyl-3-(4-chlorobenzoyl)phenyl)butanoic acidHCID 23664618Potassium methoxide

生成物 1

HCID 21495671HCID 21495671、化合物収率 72.3%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

17.5 g of 89% potassium methylate were added under an inert atmosphere to a suspension of 7.5 g of 4-(3'-p-chlorobenzoyl-2'-methyl-phenyl)-butyric acid (Example V) in 75 ml of methanol and was then heated at 120°-130° C for 17 hours under pressure. After cooling to room temperature, the mixture was rinsed with water and the methanol was eliminated under reduced pressure. The residue was dissolved in water, treated hot with activated carbon, iced and filtered. The filtrate was acidified to a pH of 1 with hydrochloric acid and the precipitate formed was recovered by filtration, was washed with water until the wash water was neutral and dried. The residue was crystallized from isopropyl ether to obtain 5.35 g of 4-(3'-p-methoxybenzoyl-2'-methyl-phenyl)-butyric acid in the form of colorless crystals melting at 100° C and then 115° C.

後処理

  1. temperaturewas then heated at 120°-130° C for 17 hours under pressure
  2. washthe mixture was rinsed with water
  3. dissolutionThe residue was dissolved in water
  4. additiontreated hot with activated carbon
  5. filtrationiced and filtered
  6. customthe precipitate formed
  7. filtrationwas recovered by filtration
  8. washwas washed with water until the wash water
  9. customdried
  10. customThe residue was crystallized from isopropyl ether

出典と根拠

ORDレコード
ord-b982dcc69d5e4b6795014530bd0c032f
出典データセット
uspto-grants-1976_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03995056

反応ノート

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