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Hydrochloric Acid → 1-(2,6-difluorobenzyl)-5-methyl-1H-1,2,3-triazole-4-carboxylic acid

HRID 414096
Notes
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Reaction equation

HRID 414096 reaction equation
[Na].[F:2][C:3]1[CH:12]=[CH:11][CH:10]=[C:9]([F:13])[C:4]=1[CH2:5][N:6]=[N+:7]=[N-:8].[C:14]([O:20]CC)(=[O:19])[CH2:15][C:16]([CH3:18])=O.[OH-].[Na+].Cl>O>[F:2][C:3]1[CH:12]=[CH:11][CH:10]=[C:9]([F:13])[C:4]=1[CH2:5][N:6]1[C:16]([CH3:18])=[C:15]([C:14]([OH:20])=[O:19])[N:8]=[N:7]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 5

HCID 313Hydrochloric AcidHCID 8868Ethyl AcetoacetateHCID 14798Sodium HydroxideHCID 5360545SodiumHCID 108883232-(Azidomethyl)-1,3-difluorobenzene

Product 1

HCID 212826091-(2,6-difluorobenzyl)-5-methyl-1H-1,2,3-triazole-4-carboxylic acid

Reagents, catalysts & solvents

1
HCID 962WaterSolvent

Procedure

The starting material is prepared as follows: 2.53 g (0.11 mole) of sodium are dissolved in 60 ml of alcohol, then a mixture of 16.9 g (0.1 mole) of 2,6-difluorobenzyl azide and 14,3 g (0.11 mole) of ethyl acetoacetat in 60 ml of alcohol is added and the batch is heated for 16 hours to reflux. After addition of 120 ml of normal sodium hydroxide solution, the reaction mixture is refluxed for another 2 hours, then diluted with 200 ml of water and acidified to pH 1 with hydrochloric acid while cooling. The precipitated product is filtered with suction, washed first with water and then with ether and dried, affording 1-(2,6-difluorobenzyl)-5-methyl-1H-1,2,3-triazole-4-carboxylic acid with a melting point of 166°-167° C.

Workup

  1. customThe starting material is prepared
  2. additionis added
  3. temperaturethe batch is heated for 16 hours
  4. temperatureto reflux
  5. temperaturethe reaction mixture is refluxed for another 2 hours
  6. temperaturewhile cooling
  7. filtrationThe precipitated product is filtered with suction
  8. washwashed first with water
  9. dry with materialwith ether and dried

Sources & evidence

ORD record
ord-8439fa910005487ea930704d99e14e44
Source dataset
uspto-grants-1988_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04789680

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes