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

HRID 414096
ノート
印刷プレビュー

反応式

HRID 414096 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 962
Water
溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-8439fa910005487ea930704d99e14e44
出典データセット
uspto-grants-1988_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04789680

反応ノート

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