Potassium Hydroxide → 5-(2-Fluorophenoxy)-2-pyrazinecarboxylic acid

HRID 2038745ノート

反応式

HRID 2038745 の反応式
C[O:2][C:3]([C:5]1[CH:10]=[N:9][C:8]([O:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[F:18])=[CH:7][N:6]=1)=[O:4].[OH-].[K+]>C(O)C>[F:18][C:13]1[CH:14]=[CH:15][CH:16]=[CH:17][C:12]=1[O:11][C:8]1[N:9]=[CH:10][C:5]([C:3]([OH:4])=[O:2])=[N:6][CH:7]=1

参加物

4

反応物 2

HCID 14797Potassium HydroxideHCID 71238257HCID 71238257、化合物

生成物 1

HCID 463182515-(2-Fluorophenoxy)-2-pyrazinecarboxylic acid収率 51.8%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

5-(2-Fluoro-phenoxy)-pyrazine-2-carboxylic acid methyl ester (Preparation 44, 57.9 g, 233 mmol) was added to a solution of KOH (15 g, 267 mmol) in 78% ethanol (330 mL). The solution was stirred at room temperature for 18 hours, and the formed precipitate was collected by filtration. The resulting solid was dissolved in water (200 mL), and the solution was acidified with aqueous hydrochloric acid. The formed precipitate was collected by filtration, dried and recrystallised from 41% ethanol (265 mL) to give the title compound (28.3 g, 120.8 mmol) in 51.8% yield.

後処理

  1. filtrationthe formed precipitate was collected by filtration
  2. dissolutionThe resulting solid was dissolved in water (200 mL)
  3. filtrationThe formed precipitate was collected by filtration
  4. customdried
  5. customrecrystallised from 41% ethanol (265 mL)

出典と根拠

ORDレコード
ord-2dabadaa01b049adadb31c39256dfca4
出典データセット
uspto-grants-2013_11
特許番号
US08575336B2

反応ノート

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