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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Trifluoroacetic acid → 5-methyl-2-oxo-2,3-dihydro-1H-imidazole-4-carboxylic acid

HRID 247593
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인쇄 미리보기

반응식

HRID 247593 반응식
CC([O:5][C:6]([C:8]1[NH:9][C:10](=[O:14])[NH:11][C:12]=1[CH3:13])=[O:7])(C)C.FC(F)(F)C(O)=O>>[CH3:13][C:12]1[NH:11][C:10](=[O:14])[NH:9][C:8]=1[C:6]([OH:7])=[O:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 6422Trifluoroacetic acidHCID 13241079HCID 13241079, 화합물

생성물 1

HCID 135585675-methyl-2-oxo-2,3-dihydro-1H-imidazole-4-carboxylic acid

실험 절차

2,3-Dihydro-5-methyl-2-oxo-1H-imidazole-4-carboxylic acid 1,1-dimethylethyl ester (110.1 g, 0.556 mol) is added in portions to stirred trifluoroacetic acid (500g). After stirring the resulting mixture at room temperature for 20 minutes the suspension is evaporated in vacuo. The solid residue is mixed with water (700 mL), the mixture filtered, and the solid residue washed with an additional portion of water (700 mL). The filter cake is then dried for 1.5 hr at ca. 105° C., then overnight at room temperature to produce the title compound.

후처리

  1. customis evaporated in vacuo
  2. additionThe solid residue is mixed with water (700 mL)
  3. filtrationthe mixture filtered
  4. washthe solid residue washed with an additional portion of water (700 mL)
  5. customThe filter cake is then dried for 1.5 hr at ca. 105° C.

출처 및 근거

ORD 기록
ord-01bef2a85dcc4de5b01f0dbe30d49a7b
출처 데이터셋
uspto-grants-1987_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04709043

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