Ethyl vinyl ether → HCID 19987079, 화합물

HRID 973904

반응식

HRID 973904 반응식
[OH:1][CH2:2][CH2:3][N:4]1[C:8](=[O:9])[CH:7]=[CH:6][C:5]1=[O:10].C(=O)([O-])[O-].[K+].[K+].[CH:17](OCC)=[CH2:18]>>[CH:17]([O:1][CH2:2][CH2:3][N:4]1[C:8](=[O:9])[CH:7]=[CH:6][C:5]1=[O:10])=[CH2:18]

참가 물질

4

실험 절차

A quantity of 1.18 g of N-(2-hydroxyethyl)maleimide was suspended in 25 ml ethyl vinyl ether and refluxed with stirring under an argon atmosphere, 70 mg mercuric acetate was added, and the reaction was continued at reflux for 24 hours. After 24 hours, the reaction mixture was allowed to cool to room temperature, and 1.50 mg of anhydrous potassium carbonate was added. After stirring for a few more minutes, the mixture was filtered and the precipitate was washed thoroughly with ethyl acetate. The washings were combined with the filtrate and evaporated to dryness in vacuo to yield an oily residue. This oily residue was chromatographed over 50 grams of neutral alumina, activity III, using methylene chloride-hexane (1:1) for elution. The initial fractions were collected and combined to yield 200 mg of crude 2-maleimidoethyl vinyl ether. The product was suitable for use in the next step in preparation of the crosslinker, but for analytical purposes could be purified by rechromatography over alumina or kugelrohr distillation.

후처리

  1. temperaturerefluxed
  2. temperatureat reflux for 24 hours
  3. stirringAfter stirring for a few more minutes
  4. filtrationthe mixture was filtered
  5. washthe precipitate was washed thoroughly with ethyl acetate
  6. customevaporated to dryness in vacuo
  7. customto yield an oily residue
  8. customThis oily residue was chromatographed over 50 grams of neutral alumina, activity III
  9. washfor elution
  10. customThe initial fractions were collected

출처 및 근거

ORD 기록
ord-626169924e0344c29b4a2ccf5bb16329
출처 데이터셋
uspto-grants-1991_11
특허 번호
US05066490

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