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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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5-Methylfurfural → 1-(5-Methylfurylideneamino)-2-oxo-imidazolidine

HRID 25926
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HRID 25926 반응식
C[C:2]1[O:3][C:4]([CH:7]=O)=[CH:5][CH:6]=1.Cl.[NH2:10][N:11]1[CH2:15][CH2:14][NH:13][C:12]1=[O:16].[OH-].[Na+]>O>[CH3:7][C:4]1[O:3][C:2](=[N:10][N:11]2[CH2:15][CH2:14][NH:13][C:12]2=[O:16])[CH2:6][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 120975-MethylfurfuralHCID 14798Sodium HydroxideHCID 192616781-Amino-2-imidazolidinone hydrochloride

생성물 1

HCID 705695311-(5-Methylfurylideneamino)-2-oxo-imidazolidine

시약·촉매·용매 1

HCID 962Water용매

실험 절차

98.3 pts. by wt. of 2-methylfuran-5-aldehyde ar added to a solution of 1-amino-2-oxo-imidazolidine hydrochloride in 1,000 pts. by vol. of water which has been brought to pH 4.5 with sodium hydroxide solution and the mixture is stirred overnight. The precipitae is filtered off, washed with water and recrystallised from ethanol. 126 pts. by wt. of 1-(5-methylfurylideneamino)-2-oxo-imidazolidine of melting point 194°-6° C. are obtained.

후처리

  1. filtrationThe precipitae is filtered off
  2. washwashed with water
  3. customrecrystallised from ethanol

출처 및 근거

ORD 기록
ord-bc74890da4ba4b8796ee9bb5340606e7
출처 데이터셋
uspto-grants-1979_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04147693

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