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Sodium Hydroxide → 3-Methoxy-2-methylbenzonitrile

HRID 1107715
ノート
印刷プレビュー

反応式

HRID 1107715 の反応式
Cl.[NH2:2]O.[CH3:4][O:5][C:6]1[C:7]([CH3:14])=[C:8]([CH:11]=[CH:12][CH:13]=1)[CH:9]=O.[OH-].[Na+]>C(O)=O>[CH3:4][O:5][C:6]1[C:7]([CH3:14])=[C:8]([CH:11]=[CH:12][CH:13]=1)[C:9]#[N:2]
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 14798Sodium HydroxideHCID 443297Hydroxyamine hydrochlorideHCID 131626633-Methoxy-2-methylbenzaldehyde

生成物 1

HCID 110947703-Methoxy-2-methylbenzonitrile収率 80%

試薬・触媒・溶媒 1

HCID 284Formic Acid溶媒

実験手順

Hydroxylamine hydrochloride (0.75 g, 11 mmol) was added to 3-methoxy-2-methylbenzaldehyde (1.25 g, 8.32 mmol) in formic acid (89-91%) (10 ml), and the mixture heated to reflux for 40 min., cooled, diluted with ice-cold water, basified with 10% aqueous sodium hydroxide solution and extracted with diethyl ether. The organic extract was washed with saturated aqueous sodium chloride (50 ml), dried over magnesium sulphate and evaporated. The residue was purified by flash chromatography over silica gel eluting with 5% diethyl ether in hexane to afford the product as a white solid (0.98 g). M+ 147; 360 MHz 1H n.m.r (CDCl3) 7.26-7.17 (2H, m), 7.02 (1H, d, J 7.9 Hz), 3.86 (3H, s), 2.41 (3H, s).

後処理

  1. temperaturethe mixture heated
  2. temperatureto reflux for 40 min.
  3. temperaturecooled
  4. additiondiluted with ice-cold water
  5. extractionextracted with diethyl ether
  6. extractionThe organic extract
  7. washwas washed with saturated aqueous sodium chloride (50 ml)
  8. dry with materialdried over magnesium sulphate
  9. customevaporated
  10. customThe residue was purified by flash chromatography over silica gel eluting with 5% diethyl ether in hexane

出典と根拠

ORDレコード
ord-9f70d035c6c641d08f2557ab721148a2
出典データセット
uspto-grants-2000_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06063789

反応ノート

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