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Formic Acid → Methyl 5-formylpyrrole-3-carboxylate

HRID 1381099
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HRID 1381099 반응식
[CH3:1][O:2][C:3]([C:5]1[CH:6]=[C:7]([C:10]#N)[NH:8][CH:9]=1)=[O:4].C(O)=[O:13]>[Ni]>[CH3:1][O:2][C:3]([C:5]1[CH:6]=[C:7]([CH:10]=[O:13])[NH:8][CH:9]=1)=[O:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 284Formic AcidHCID 12415103methyl 5-cyano-1H-pyrrole-3-carboxylate

생성물 1

HCID 579027Methyl 5-formylpyrrole-3-carboxylate수율 36%

시약·촉매·용매 1

HCID 935Nickel촉매

실험 절차

3.6 g (27 millimoles) of 2-cyanopyrrole-4-carboxylic acid methyl ester, 17 g of Raney nickel, and 450 ml of 75% formic acid are introduced, in a flask, into an oil bath preheated to 120° C. and made to react for one hour. Subsequently, the mixture is poured into 1 liter of ice water and repeatedly extracted with ether. After drying and concentration of the ether phase, 1.4 g (36% of theory) of 2-formylpyrrole-4-carboxylic acid methyl ester is obtained, mp 126° C.

후처리

  1. custompreheated to 120° C.
  2. customto react for one hour
  3. extractionrepeatedly extracted with ether
  4. customAfter drying

출처 및 근거

ORD 기록
ord-60fdaed4569749c988842a25fa64e6e7
출처 데이터셋
uspto-grants-1986_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04585771

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