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Ethyl 2-chloroacetoacetate → HCID 178418931, compound

HRID 11196
Notes
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Reaction equation

HRID 11196 reaction equation
[NH2:1][C:2]1[N:6]=[CH:5][NH:4][N:3]=1.C([O:9][C:10](=O)[CH:11]([Cl:15])[C:12]([CH3:14])=O)C>C(O)(=O)C.CCOCC.CO.CN(C=O)C.CS(C)=O>[Cl:15][C:11]1[C:12]([CH3:14])=[N:1][C:2]2[N:3]([N:4]=[CH:5][N:6]=2)[C:10]=1[OH:9]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 2

HCID 11858Ethyl 2-chloroacetoacetateHCID 178418311HCID 178418311, compound

Product 1

HCID 178418931HCID 178418931, compound

Reagents, catalysts & solvents 4

HCID 176Acetic AcidSolventHCID 679Dimethyl SulfoxideSolventHCID 6228Dimethylformamide
Solvent
HCID 21864698Diethyl ether methanolSolvent

Procedure

3-Amino-1,2,4-triazole (4.2 g, 0.05 mol) and ethyl-2-chloro-acetoacetate (12.64 g, 0.0768 mol) were refluxed in acetic acid (15 ml) under a nitrogen atmosphere. The reaction mixture first turned into a clear yellow solution and after about 15 minutes a solid started precipitating. Reflux continued for one hour. The crude product was filtered off, washed with hot methanol (2×10 ml), and dried in an oven at 90° C. to give 5.9 g (64%) of pure TAI-3. TLC (in Et2O/MeOH, 70:30 v/v) showed only one spot. The compound is soluble in hot DMF and DMSO. mp=starts darkening at ˜308° C. and decomposes at temperatures >325° C.

Workup

  1. customa solid started precipitating
  2. temperatureReflux
  3. waitcontinued for one hour
  4. filtrationThe crude product was filtered off
  5. washwashed with hot methanol (2×10 ml)
  6. customdried in an oven at 90° C.
  7. customto give 5.9 g (64%) of pure TAI-3
  8. customstarts darkening at ˜308° C.
  9. customdecomposes at temperatures >325° C.

Sources & evidence

ORD record
ord-55ee4330953246a9a99fcfd9784870dc
Source dataset
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07097963B1

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes