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Methanol → 2-Propenoic acid, 3-(4-fluorophenyl)-, methyl ester

HRID 256705
ノート
印刷プレビュー

反応式

HRID 256705 の反応式
[F:1][C:2]1[CH:12]=[CH:11][C:5]([CH:6]=[CH:7][C:8]([OH:10])=[O:9])=[CH:4][CH:3]=1.[CH3:13]O.S(=O)(=O)(O)O.O>C(OCC)C>[CH3:13][O:9][C:8](=[O:10])[CH:7]=[CH:6][C:5]1[CH:4]=[CH:3][C:2]([F:1])=[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

6

反応物 4

HCID 887Methanol2 回HCID 962WaterHCID 1118Sulfuric AcidHCID 980703-(4-Fluorophenyl)-2-propenoic acid

生成物 1

HCID 9587502-Propenoic acid, 3-(4-fluorophenyl)-, methyl ester

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

A one liter round bottom flask was charged with 50 grams (0.30 moles) of 4-fluorocinnamic acid, 500 milliliters of methanol, and 5.0 grams of concentrated sulfuric acid. This mixture was brought to reflux and kept there for 18 hours. After cooling, one half of the methanol was stripped under vacuum, and the remaining solution was poured into 600 milliliters of water. The precipitated solid was taken into 500 milliliters of diethyl ether and the aqueous phase was discarded. The ether solution was washed three times with 10% aqueous sodium hydroxide and once with water. After drying over magnesium sulfate, the mixture was filtered and stripped under vacuum to give methyl-4-fluorocinnamate as a white crystalline powder. Yield was 40 grams.

後処理

  1. temperatureto reflux
  2. temperatureAfter cooling
  3. washThe ether solution was washed three times with 10% aqueous sodium hydroxide
  4. dry with materialAfter drying over magnesium sulfate
  5. filtrationthe mixture was filtered

出典と根拠

ORDレコード
ord-cfb318807128447bb7fd55580030b7a4
出典データセット
uspto-grants-1993_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05258517

反応ノート

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