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Hydroxyamine hydrochloride → HCID 86659950、化合物

HRID 1804521
ノート
印刷プレビュー

反応式

HRID 1804521 の反応式
[CH3:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[C:4]([C:10]([F:13])([F:12])[F:11])[CH:3]=1.Cl.[NH2:15][OH:16].C(=O)(O)[O-].[Na+]>CO>[OH:16][N:15]=[C:6]([NH2:7])[C:5]1[CH:8]=[CH:9][C:2]([CH3:1])=[CH:3][C:4]=1[C:10]([F:13])([F:11])[F:12]
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 443297Hydroxyamine hydrochlorideHCID 516892Sodium BicarbonateHCID 27755974-Methyl-2-(trifluoromethyl)benzonitrile

生成物 1

HCID 86659950HCID 86659950、化合物収率 45.4%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

An oven-dried 20 mL reaction vial containing a stir bar was cooled under a stream of dry nitrogen. The vial was charged with 4-methyl-2-(trifluoromethyl)benzonitrile (1000 mg, 5.40 mmol), hydroxylamine hydrochloride (469 mg, 6.75 mmol), sodium bicarbonate (681 mg, 8.10 mmol), and methanol (6 mL). The vial was flushed with nitrogen, sealed, stirred at room temperature for 30 minutes, and then placed in a sand bath set to 75° C. and stirred overnight. The crude reaction material was purified by reverse phase preparative HPLC. The collected product fractions were evaporated under vacuum to afford N′-hydroxy-4-methyl-2-(trifluoromethyl)benzimidamide (0.54 g, 2.45 mmol, 45% yield). MS M+1=219.0.

後処理

  1. customAn oven-dried 20 mL reaction
  2. additionvial containing a stir bar
  3. temperaturewas cooled under a stream of dry nitrogen
  4. customThe vial was flushed with nitrogen
  5. customsealed
  6. customplaced in a sand bath
  7. customset to 75° C.
  8. stirringstirred overnight
  9. customThe crude reaction material
  10. customwas purified by reverse phase preparative HPLC
  11. customThe collected product fractions were evaporated under vacuum

出典と根拠

ORDレコード
ord-2c8cbcfb06914b3baf4cd253207fcdfb
出典データセット
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08354398B2

反応ノート

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