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Methanol → 5-(4-Fluoro-phenyl)-pentanoic acid methyl ester

HRID 2100506
ノート
印刷プレビュー

反応式

HRID 2100506 の反応式
S(Cl)(Cl)=O.[F:5][C:6]1[CH:11]=[CH:10][C:9]([CH2:12][CH2:13][CH2:14][CH2:15][C:16]([OH:18])=[O:17])=[CH:8][CH:7]=1.O.[CH3:20]O>>[CH3:20][O:17][C:16](=[O:18])[CH2:15][CH2:14][CH2:13][CH2:12][C:9]1[CH:8]=[CH:7][C:6]([F:5])=[CH:11][CH:10]=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 4

HCID 887MethanolHCID 962WaterHCID 24386Thionyl ChlorideHCID 27346705-(4-Fluorophenyl)pentanoic acid

生成物 1

HCID 685705095-(4-Fluoro-phenyl)-pentanoic acid methyl ester収率 75%

実験手順

Thionylchloride (288 μl, 3.98 mmol) was added dropwise to a solution of 5-(4-fluoro-phenyl)-pentanoic acid (520 mg, 2.65 mmol) in methanol (11 ml) at −15° C. The reaction mixture was then stirred at room temperature for 1.5 h. Water was added and the mixture was extracted 3 times with diethylether. The combined extracts were washed with water and brine, dried (Na2SO4) and evaporated. The remaining residue was purified by column chromatography (silica gel, ethyl acetate/heptane 5:95 to 12:88) to obtain 5-(4-fluoro-phenyl)-pentanoic acid methyl ester (420 mg, 2 mmol; 75%) as colorless liquid. MS: m/e 211.0 [M+H+].

後処理

  1. extractionthe mixture was extracted 3 times with diethylether
  2. washThe combined extracts were washed with water and brine
  3. dry with materialdried (Na2SO4)
  4. customevaporated
  5. customThe remaining residue was purified by column chromatography (silica gel, ethyl acetate/heptane 5:95 to 12:88)

出典と根拠

ORDレコード
ord-27480444f9d347468d44545597e2c8dc
出典データセット
uspto-grants-2009_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07572801B2

反応ノート

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