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Chloroacetic Acid → [2-(2-Methoxyphenyl)ethoxy]acetic acid

HRID 1712319
ノート
印刷プレビュー

反応式

HRID 1712319 の反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[CH2:9][CH2:10][OH:11].[H-].[Na+].Cl[CH2:15][C:16]([OH:18])=[O:17]>CS(C)=O>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[CH2:9][CH2:10][O:11][CH2:15][C:16]([OH:18])=[O:17]
参加物反応条件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 300Chloroacetic AcidHCID 24758Sodium hydrideHCID 819092-Methoxyphenethyl alcohol

生成物 1

HCID 24769570[2-(2-Methoxyphenyl)ethoxy]acetic acid

試薬・触媒・溶媒 1

HCID 679Dimethyl Sulfoxide溶媒

反応条件

温度
60 °C

実験手順

The solution of 10.0 g of 2-(2-methoxyphenyl)ethanol in 130 ml of dimethyl sulphoxide is admixed with stirring with sodium hydride dispersion (60%) and stirred at 60° C. over 10 min. The suspension is admixed slowly with 6.20 g of chloroacetic acid and subsequently stirred at 80° C. over 2 hours. The reaction mixture is cooled, poured onto ice-water (0.5 l) and washed with ethyl acetate (1×250 ml). The aqueous phase is acidified with 2M HCl and extracted with ethyl acetate (2×250 ml). The organic phases are washed successively with water (250 ml) and brine (1×250 ml), dried over sodium sulphate, filtered and concentrated. The title compound is obtained as a slightly yellowish oil from the residue by means of flash chromatography (SiO2 60F). Rf=0.04 (200:20:1 dichloromethane-methanol-conc. ammonia); Rt=3.44.

後処理

  1. stirringsubsequently stirred at 80° C. over 2 hours
  2. temperatureThe reaction mixture is cooled
  3. additionpoured onto ice-water (0.5 l)
  4. washwashed with ethyl acetate (1×250 ml)
  5. extractionextracted with ethyl acetate (2×250 ml)
  6. washThe organic phases are washed successively with water (250 ml) and brine (1×250 ml)
  7. dry with materialdried over sodium sulphate
  8. filtrationfiltered
  9. concentrationconcentrated

出典と根拠

ORDレコード
ord-4fdc2a4eb04147769a9bca4873110804
出典データセット
uspto-grants-2010_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07790715B2

反応ノート

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