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Hydrochloric Acid → 3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxylic acid

HRID 1411110
ノート
印刷プレビュー

反応式

HRID 1411110 の反応式
[OH-:1].[Na+].[F:3][CH:4]([F:15])[C:5]1[C:9]([C:10](F)=[O:11])=[C:8]([F:13])[N:7]([CH3:14])[N:6]=1.Cl>S1(=O)(=O)CCCC1>[F:13][C:8]1[N:7]([CH3:14])[N:6]=[C:5]([CH:4]([F:15])[F:3])[C:9]=1[C:10]([OH:1])=[O:11]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 585266223-(Difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carbonyl fluoride

生成物 1

HCID 231925843-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxylic acid

試薬・触媒・溶媒 1

HCID 31347Sulfolane溶媒

実験手順

To 400 ml of a 1N sodium hydroxide aqueous solution, was added dropwise 67.5 g of a solution (10% molar) of 3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carbonyl fluoride in tetrahydrothiophene 1,1-dioxide. The temperature was kept below 20° C. during the addition. After 2 hours of stirring at room temperature, the reaction mixture was carefully acidified to pH 2 with concentrated aqueous hydrochloric acid. The resulting white precipitate was filtered, washed with water, and dried to yield 6 g of 5-fluoro-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylic acid as a white solid.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. additionThe temperature was kept below 20° C. during the addition
  2. filtrationThe resulting white precipitate was filtered
  3. washwashed with water
  4. customdried

出典と根拠

ORDレコード
ord-14db3cd7850342548f755ef605addacd
出典データセット
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08921575B2

反応ノート

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