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Sulfuric Acid → Methyl 1-(4-fluorophenyl)cyclopentanecarboxylate

HRID 28773
ノート
印刷プレビュー

反応式

HRID 28773 の反応式
C[CH:2]1[CH2:6][CH2:5][CH2:4][C:3]1([C:10]1[CH:15]=[CH:14][C:13]([F:16])=[CH:12][CH:11]=1)[C:7]([OH:9])=[O:8].S(=O)(=O)(O)O.[C:22](=O)([O-])[O-].[Na+].[Na+]>CO>[F:16][C:13]1[CH:14]=[CH:15][C:10]([C:3]2([C:7]([O:9][CH3:22])=[O:8])[CH2:4][CH2:5][CH2:6][CH2:2]2)=[CH:11][CH:12]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 1118Sulfuric AcidHCID 10340Sodium CarbonateHCID 69250985Methyl 1-(4-fluorophenyl)cyclopentanecarboxylic acid

生成物 1

HCID 20110263Methyl 1-(4-fluorophenyl)cyclopentanecarboxylate

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a solution of methyl 1-(4-fluorophenyl)cyclopentanecarboxylic acid (5.0 g, 24.01 mmol) in anhydrous methanol was added 1 mL of the concentration of sulfuric acid. The mixture was refluxed for overnight. The mixture was neutralized to pH 4-5 with sodium carbonate. The solvent was evaporated. The residue was dissolved in ethyl acetate (50 mL), washed with brine (3×10 mL), dried over MgSO4. The crude product was used for the next reaction without further purification.

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. temperatureThe mixture was refluxed for overnight
  2. customThe solvent was evaporated
  3. dissolutionThe residue was dissolved in ethyl acetate (50 mL)
  4. washwashed with brine (3×10 mL)
  5. dry with materialdried over MgSO4
  6. customThe crude product was used for the next reaction without further purification

出典と根拠

ORDレコード
ord-2c94fa4bf6ab424fa0b09a01ed9c37b1
出典データセット
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07419999B2

反応ノート

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