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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Itaconic acid → HCID 86658305, 화합물

HRID 2402762
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HRID 2402762 반응식
[C:1]([OH:9])(=[O:8])[C:2]([CH2:4][C:5]([OH:7])=[O:6])=[CH2:3].CN.C(C1C[N:18](C)[C:17](=O)C1)(O)=O>O>[C:1]([OH:9])(=[O:8])[C:2]([CH2:4][C:5]([OH:7])=[O:6])=[CH2:3].[CH3:17][NH2:18]
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참가 물질

5

반응물 3

HCID 811Itaconic acid2회HCID 6329MethylamineHCID 1227661-Methyl-5-oxopyrrolidine-3-carboxylic acid

생성물 1

HCID 86658305HCID 86658305, 화합물수율 67%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

Itaconic acid (100 g, 0.78 mol) and methylamine (41% in water, 60.0 g based on the aqueous solution, 0.80 mol, 1.0 equivalent) were mixed as in example 8. The suspension was heated to boiling under reflux at standard pressure for 1 hour (in the course of which the boiling point rises to approx. 115° C.). This dissolved the solids completely. Cooling to ambient temperature formed a precipitate. NMR analysis of the homogeneous solution and of the precipitated crystals (solvent: D2O) showed that the itaconic acid:4-carboxy-1-methylpyrrolidone ratio in both phases was 0:100. The 4-carboxy-1-methylpyrrolidone product was purified by recrystallization from ethyl acetate and was obtained in the form of colorless crystals (yield: 59 g, 67%).

후처리

  1. additionwere mixed as in example 8
  2. temperatureThe suspension was heated
  3. temperatureunder reflux at standard pressure for 1 hour (in the course of which the boiling point
  4. customrises to approx. 115° C.
  5. dissolutionThis dissolved the solids completely
  6. customformed a precipitate
  7. customThe 4-carboxy-1-methylpyrrolidone product was purified by recrystallization from ethyl acetate

출처 및 근거

ORD 기록
ord-6eb2071a5ea64ffb98dd51b68213eff3
출처 데이터셋
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08796472B2

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