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Sodium Hydroxide → 4-Methyl-2-phenylpentanoic acid

HRID 902746
ノート
印刷プレビュー

反応式

HRID 902746 の反応式
C[C:2]([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)([CH2:6][C:7]([CH3:9])=[CH2:8])[C:3]([OH:5])=[O:4].[OH-].[Na+]>O>[C:10]1([CH:2]([CH2:6][CH:7]([CH3:9])[CH3:8])[C:3]([OH:5])=[O:4])[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=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 14798Sodium HydroxideHCID 69253057Methyl 2-phenyl-4-methyl-4-pentenoic Acid

生成物 1

HCID 2365774-Methyl-2-phenylpentanoic acid

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

A solution of methyl 2-phenyl-4-methyl-4-pentenoic acid (850 mg, 4.15 mmole) in 10 mL of MeOHwas treated with 5 mL of 2.5N NaOH and heated to 50° for 30 minutes. The reaction was cooled, diluted with H2O and washed with Et2O. The aqueous phase was acified, and extracted with CH2Cl2. The extracts were washed with H2O, dried and the solvent removed. The residue was dissolved in 25 mL of EtOAc, and hydrogenated over a 10% Pd/C catalyst, at 1 atmosphere H2 pressure, for 2 hours. The catalyst was filtered and the solvent removed and gave the titled compound, 647 mg (81%). MS (ESI) 193 (MH+)

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. temperatureheated to 50° for 30 minutes
  2. temperatureThe reaction was cooled
  3. washwashed with Et2O
  4. extractionextracted with CH2Cl2
  5. washThe extracts were washed with H2O
  6. customdried
  7. customthe solvent removed
  8. dissolutionThe residue was dissolved in 25 mL of EtOAc
  9. filtrationThe catalyst was filtered
  10. customthe solvent removed

出典と根拠

ORDレコード
ord-963f3a8ff95a4f48950097331f079fa7
出典データセット
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07365085B2

反応ノート

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