Water → Ethyl 3-bromobenzyloxyacetate

HRID 54192

反応式

HRID 54192 の反応式
[Br:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH2:5][OH:6].Br[CH2:11][C:12]([O:14][CH2:15][CH3:16])=[O:13].O>CN(C)C=O>[Br:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH2:5][O:6][CH2:11][C:12]([O:14][CH2:15][CH3:16])=[O:13]

参加物

5

実験手順

Part A: 3-Bromobenzyl alcohol (2.0 g) was dissolved in dimethyl formamide (50 ml) in a dry 100 ml flask under nitrogen. Sodium hydride (0.5 g of a 60% suspension in mineral oil, washed with hexane, 11.8 mmol) was added in portions and the mixture was stirred for one hour at room temperature. Ethyl bromoacetate (1.2 ml, 11.8 mmol) was added drop-wise and the reaction was stirred overnight at room temperature then mixed with water (150 ml) and extracted with methylene chloride (3×20 ml). The extracts were combined, washed with water (50 ml), saturated sodium chloride solution (50 ml) and then dried (MgSO4). The solution was filtered and concentrated and the residue was purified by flash chromatography (SiO2, gradient hexane to ethyl acetate) which gave 2.35 g (80%) of ethyl 3-bromobenzyloxyacetate as an oil.

後処理

  1. washSodium hydride (0.5 g of a 60% suspension in mineral oil, washed with hexane, 11.8 mmol)
  2. additionwas added in portions
  3. stirringthe reaction was stirred overnight at room temperature
  4. extractionextracted with methylene chloride (3×20 ml)
  5. washwashed with water (50 ml), saturated sodium chloride solution (50 ml)
  6. dry with materialdried (MgSO4)
  7. filtrationThe solution was filtered
  8. concentrationconcentrated
  9. customthe residue was purified by flash chromatography (SiO2, gradient hexane to ethyl acetate) which

出典と根拠

ORDレコード
ord-4ee2eba34d474c2499c65a8ee03e448f
出典データセット
uspto-grants-1997_04
特許番号
US05622937

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