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Malonic Acid → (E)-3-(6-Acetamidopyridin-3-YL)acrylic acid

HRID 581785
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인쇄 미리보기

반응식

HRID 581785 반응식
[C:1]([NH:4][C:5]1[CH:10]=[CH:9][C:8]([CH:11]=O)=[CH:7][N:6]=1)(=[O:3])[CH3:2].C(O)(=O)[CH2:14][C:15]([OH:17])=[O:16]>N1C=CC=CC=1.C(O)C>[C:1]([NH:4][C:5]1[N:6]=[CH:7][C:8](/[CH:11]=[CH:14]/[C:15]([OH:17])=[O:16])=[CH:9][CH:10]=1)(=[O:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 867Malonic AcidHCID 22113222N-(5-Formylpyridin-2-yl)acetamide

생성물 1

HCID 10703461(E)-3-(6-Acetamidopyridin-3-YL)acrylic acid수율 81.9%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 1049Pyridine용매

실험 절차

A mixture of 2-acetylamino-5-formylpyridine (241 mg) and malonic acid (168 mg) in pyridine (0.12 ml) and ethanol (0.36 ml) was refluxed for 2 hours. After cooling the mixture, the precipitate was collected by filtration, and washed with ethyl acetate to give (E)-3-(6-acetylamino-3-pyridyl)acrylic acid (248 mg) as a colorless powder. mp: 291-2920° C.

후처리

  1. temperaturewas refluxed for 2 hours
  2. temperatureAfter cooling the mixture
  3. filtrationthe precipitate was collected by filtration
  4. washwashed with ethyl acetate

출처 및 근거

ORD 기록
ord-a2977919b0654270b5d9e948b1dd9aab
출처 데이터셋
uspto-grants-1999_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05922711

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