Chloroacetic Acid → 2-(2-Phenylethoxy)acetic acid

HRID 530517ノート

反応式

HRID 530517 の反応式
[CH2:1]([OH:9])[CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[H-].[Na+].Cl[CH2:13][C:14]([OH:16])=[O:15].Cl>CS(C)=O.O>[CH2:1]([O:9][CH2:13][C:14]([OH:16])=[O:15])[CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1

参加物

7

反応条件

温度
60 °C

実験手順

To a stirred mixture of phenethyl alcohol (1.0 g, 8.18 mmol) in DMSO (16 mL) under nitrogen flow, NaH (0.39 g, 16.37 mmol) was added in one portion and the mixture was stirred at 60° C. for 10 min. Following the addition of chloroacetic acid (0.77 g, 8.18 mmol), the reaction mixture was heated at 80° C. for 3 h. The cooled mixture was then poured into H2O and the aqueous phase acidified to pH 1.0 with a 2.0 N HCl solution. The aqueous phase was then extracted with EtOAc (3×20 mL), and the combined organic phase washed with brine and dried over Na2SO4 to afford the title compound (1.11 g, 75%), which was used in the following step without further purification. 1H NMR (DMSO-d6): δ 2.83 (t, J=7.0 Hz, 2H), 3.67 (t, J=7.0 Hz, 2H), 4.00 (s, 2H), 7.15-7.32 (m, 5H), 12.64 (s, 1H).

後処理

  1. additionwas added in one portion
  2. temperaturethe reaction mixture was heated at 80° C. for 3 h
  3. extractionThe aqueous phase was then extracted with EtOAc (3×20 mL)
  4. washthe combined organic phase washed with brine
  5. dry with materialdried over Na2SO4

出典と根拠

ORDレコード
ord-01c5c7980a224801904c49fc7201d7e3
出典データセット
uspto-grants-2016_05
特許番号
US09353075B2

反応ノート

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