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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Carbon Dioxide → HCID 68117788, 화합물

HRID 597656
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HRID 597656 반응식
[C:1]([O:4][C:5]1[CH:19]=[CH:18][C:8]([CH:9]=[C:10]([NH:14][C:15](=[O:17])[CH3:16])C(O)=O)=[CH:7][C:6]=1OC)(=[O:3])[CH3:2].[C:22](=O)=[O:23]>[Cu].N1C2C(=CC=CC=2)C=CC=1>[C:15]([NH:14][CH:10]=[CH:9][C:8]1[CH:7]=[CH:6][C:5]([O:4][C:1](=[O:3])[CH2:2][O:23][CH3:22])=[CH:19][CH:18]=1)(=[O:17])[CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 280Carbon DioxideHCID 27543002-(Acetylamino)-3-[4-(acetyloxy)-3-methoxyphenyl]-2-propenoic acid

생성물 1

HCID 68117788HCID 68117788, 화합물

시약·촉매·용매 2

HCID 23978Copper촉매HCID 7047Quinoline용매

실험 절차

18.0 g (0.06 mol) of 4-acetoxy-α-acetylamino-3-methoxy-cinnamic acid are heated with 30 ml of quinoline and 1.2 g of copper powder to 160°-170° C for 3 hours, in the course of which carbon dioxide is evolved. Thereafter, the quinoline is distilled off under reduced pressure and the residual mass is taken up in ethyl acetate. After filtering off the copper powder, the ethyl acetate solution is extracted with 25 ml of 1 N hydrochloric acid and is then washed with water and subsequently with sodium bicarbonate solution. The organic phase is dried over sodium sulphate and thereafter the solvent is removed by distillation under reduced pressure. The resulting oil yields 4-(2-acetylaminovinyl)-2-methoxy-acetoxy-benzene, of melting point 169°-170° C, from ethyl acetate.

후처리

  1. distillationThereafter, the quinoline is distilled off under reduced pressure
  2. filtrationAfter filtering off the copper powder
  3. extractionthe ethyl acetate solution is extracted with 25 ml of 1 N hydrochloric acid
  4. washis then washed with water and subsequently with sodium bicarbonate solution
  5. dry with materialThe organic phase is dried over sodium sulphate
  6. customthe solvent is removed by distillation under reduced pressure

출처 및 근거

ORD 기록
ord-8a5624b696ed48938d95beb7a3d3c9c4
출처 데이터셋
uspto-grants-1977_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04014920

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