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Hydrochloric Acid → Benzeneacetic acid, alpha-ethyl-, methyl ester

HRID 494600
ノート
印刷プレビュー

反応式

HRID 494600 の反応式
[C:1]1([CH:7]([CH2:11][CH3:12])[C:8]([OH:10])=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Cl.[CH3:14]O>>[C:1]1([CH:7]([CH2:11][CH3:12])[C:8]([O:10][CH3:14])=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=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 3

HCID 313Hydrochloric AcidHCID 887MethanolHCID 70122-Phenylbutyric Acid

生成物 1

HCID 102780Benzeneacetic acid, alpha-ethyl-, methyl ester

実験手順

2-Phenylbutyric acid (10 g, 61 mmole) was dissolved in methanol (30 ml) treated with concentrated HCl (1 ml) and heated at reflux for 20 hours. The heating was stopped and the reaction mixture cooled to room temperature. The solvent was removed in vacuo and the oily residue was treated with ethyl acetate (100 ml). The organic layer was washed with saturated sodium bicarbonate solution and saturated sodium chloride solution, dried (Na2SO4), filtered and concentrated in vacuo to give the title compound as a clear oil. Yield 10.61 g (97%). 1H NMR (300 MHz, DMSO-d6): δ ppm 0.81 (t, J=7.35 Hz, 3H) 1.69 (m, 1H) 1.98 (m, 1H) 3.53 (d, J=7.35 Hz, 1H) 3.58 (s, 3H) 7.30 (m, 5H).

後処理

  • temperatureheated
  • temperatureat reflux for 20 hours
  • customThe solvent was removed in vacuo
  • additionthe oily residue was treated with ethyl acetate (100 ml)
  • washThe organic layer was washed with saturated sodium bicarbonate solution and saturated sodium chloride solution
  • dry with materialdried (Na2SO4)
  • filtrationfiltered
  • concentrationconcentrated in vacuo
  • 出典と根拠

    ORDレコード
    ord-839125d2cbb44722ad98420b53950150
    出典データセット
    uspto-grants-2009_05
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US07538105B2

    反応ノート

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