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Allyl Alcohol → 2-Chloro-3-[(prop-2-en-1-yl)oxy]pyrazine

HRID 1701740
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HRID 1701740 반응식
Cl[C:2]1[C:7]([Cl:8])=[N:6][CH:5]=[CH:4][N:3]=1.[CH2:9]([OH:12])[CH:10]=[CH2:11].[H-].[Na+]>CS(C)=O>[CH2:9]([O:12][C:2]1[C:7]([Cl:8])=[N:6][CH:5]=[CH:4][N:3]=1)[CH:10]=[CH2:11]
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참가 물질

5

반응물 3

HCID 7858Allyl AlcoholHCID 24758Sodium hydrideHCID 785752,3-Dichloropyrazine

생성물 1

HCID 136828382-Chloro-3-[(prop-2-en-1-yl)oxy]pyrazine

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

59.6 g of 2,3-dichloropyrazine and 92.8 g of allyl alcohol are dissolved in 400 ml of dimethylsulphoxide. 9.6 g of sodium hydride are introduced into this solution over the course of 30 minutes at 0°-5° C., whilst stirring. The mixture is then stirred for 15 hours at room temperature. Thereafter the reaction mixture is poured into 2 liters of ice water and extracted by shaking with ether. The ether extracts are washed with water, dried over sodium sulphate and evaporated in a waterpump vacuum. The residue is distilled in a high vacuum. 2-Allyloxy-3-chloro-pyrazine, boiling point 42°-44° C./0.03 mm Hg, is thus obtained.

후처리

  1. stirringThe mixture is then stirred for 15 hours at room temperature
  2. extractionextracted
  3. stirringby shaking with ether
  4. washThe ether extracts are washed with water
  5. dry with materialdried over sodium sulphate
  6. customevaporated in a waterpump vacuum
  7. distillationThe residue is distilled in a high vacuum

출처 및 근거

ORD 기록
ord-ae20242a2ece4a3993ee0974b4a10122
출처 데이터셋
uspto-grants-1980_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04195090

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