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5-Methylfurfural → 1-(5-Methylfurylideneamino)-2-oxo-imidazolidine

HRID 25926
Notes
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Reaction equation

HRID 25926 reaction equation
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
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

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

Product 1

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

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

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.

Workup

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

Sources & evidence

ORD record
ord-bc74890da4ba4b8796ee9bb5340606e7
Source dataset
uspto-grants-1979_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04147693

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes