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Sodium Hydroxide → 2-chloro-6-fluoro-4-(1H-pyrazol-3-yl)benzonitrile

HRID 1409311
ノート
印刷プレビュー

反応式

HRID 1409311 の反応式
Cl.[Cl:2][C:3]1[CH:10]=[C:9]([C:11]2[NH:15][N:14]=[CH:13][CH:12]=2)[CH:8]=[C:7]([F:16])[C:4]=1[C:5]#[N:6].[OH-].[Na+]>C1COCC1>[Cl:2][C:3]1[CH:10]=[C:9]([C:11]2[NH:15][N:14]=[CH:13][CH:12]=2)[CH:8]=[C:7]([F:16])[C:4]=1[C:5]#[N:6]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 14798Sodium HydroxideHCID 709807222-Chloro-6-fluoro-4-(1H-pyrazol-5-yl)benzonitrile hydrochloride

生成物 1

HCID 671697812-chloro-6-fluoro-4-(1H-pyrazol-3-yl)benzonitrile収率 80.4%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

2-Chloro-6-fluoro-4-(1H-pyrazol-5-yl)benzonitrile hydrochloride (201 mmol, 51.8 g) was dissolved in THF (510 ml). Sodium hydroxide 50% (401 mmol, 32.1 g) was added and the resulting mixture was stirred at RT for 3 h. Almost all the solvents were evaporated and water was added to the residue. The mixture was stirred overnight at RT. The precipitate was removed by filtration the solid was flushed twice with water. The solid was dried under vacuum. 35.8 g of the title compound was obtained. 1H-NMR (400 MHz, DMSO-d6): δ 7.05 (d, 1H), 7.88-7.97 (m, 2H), 8.02-8.07 (m, 1H), 13.37 (bs, 1H).

後処理

  1. customAlmost all the solvents were evaporated
  2. additionwater was added to the residue
  3. stirringThe mixture was stirred overnight at RT
  4. customThe precipitate was removed by filtration the solid
  5. customwas flushed twice with water
  6. customThe solid was dried under vacuum

出典と根拠

ORDレコード
ord-5ad683de8ee8439bae3d68b9104896b2
出典データセット
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08921378B2

反応ノート

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