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Water → 3-(4-Fluorophenyl)-6-methylpicolinic acid

HRID 61004
ノート
印刷プレビュー

反応式

HRID 61004 の反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:9]([C:15]#N)=[N:10][C:11]([CH3:14])=[CH:12][CH:13]=2)=[CH:4][CH:3]=1.[OH-:17].[Na+].[OH2:19]>CO>[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:9]([C:15]([OH:19])=[O:17])=[N:10][C:11]([CH3:14])=[CH:12][CH:13]=2)=[CH:4][CH:3]=1
参加物反応条件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 962WaterHCID 14798Sodium HydroxideHCID 1177278303-(4-Fluorophenyl)-6-methylpicolinonitrile

生成物 1

HCID 674203323-(4-Fluorophenyl)-6-methylpicolinic acid

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
100 °C

実験手順

To the solution of 3-(4-fluorophenyl)-6-methylpicolinonitrile (0.555 g, 2.615 mmol) in MeOH (3 mL) was added NaOH (1.1 g, 27.5 mmol) and H2O (1.8 mL). The mixture was heated at 100° C. for 8 h. The reaction was cooled to rt and acidified to pH-5. The solvent was removed in vacuo. The crude was extracted with MeOH. The solvent was removed in vacuo and the obtained acid was dried in vacuum for next step with no further purification. ESI-MS (m/z): 233 [M+1]+.

後処理

  1. temperatureThe reaction was cooled to rt
  2. customThe solvent was removed in vacuo
  3. extractionThe crude was extracted with MeOH
  4. customThe solvent was removed in vacuo
  5. customthe obtained acid was dried in vacuum for next step with no further purification

出典と根拠

ORDレコード
ord-db06a1b42d6e4a128ca34831ff6e42a1
出典データセット
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09440982B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート