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Hydroxylamine → 2-Benzyloxy-3,4-dimethoxybenzonitrile

HRID 1004017
ノート
印刷プレビュー

反応式

HRID 1004017 の反応式
C([O-])(=O)C.[Na+].[NH2:6]O.[CH2:8]([O:15][C:16]1[C:23]([O:24][CH3:25])=[C:22]([O:26][CH3:27])[CH:21]=[CH:20][C:17]=1[CH:18]=O)[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.O>C(O)(=O)C>[CH2:8]([O:15][C:16]1[C:23]([O:24][CH3:25])=[C:22]([O:26][CH3:27])[CH:21]=[CH:20][C:17]=1[C:18]#[N:6])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 787HydroxylamineHCID 962WaterHCID 517045Sodium AcetateHCID 8195792-(Benzyloxy)-3,4-dimethoxybenzaldehyde

生成物 1

HCID 184706112-Benzyloxy-3,4-dimethoxybenzonitrile

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

実験手順

A slurry of sodium acetate (17.06 g, 0.208 mol) and hydroxylamine (14.45 g, 0.208 mol) in glacial acetic acid (120 ml) was added to 2-benzyloxy-3,4-dimethoxybenzaldehyde (28.3 g, 0.104 mol) and the resulting suspension stirred at reflux for 18 hours. On cooling, water (250 ml) was added and the mixture extracted with dichloromethane (500 ml). The combined organic extracts were dried (MgSO4), filtered and evaporated under reduced pressure. The crude product was purified on silica gel eluting with hexane:ethyl acetate (80:20 v/v) to give the subtitle compound as an oil that crystallised on standing (21.06 g, 75%). Rf 0.52 (ethyl acetate:hexane, 1:1, v/v). MS m/z 270 (MH)+.

後処理

  1. temperatureat reflux for 18 hours
  2. temperatureOn cooling
  3. extractionthe mixture extracted with dichloromethane (500 ml)
  4. dry with materialThe combined organic extracts were dried (MgSO4)
  5. filtrationfiltered
  6. customevaporated under reduced pressure
  7. customThe crude product was purified on silica gel eluting with hexane:ethyl acetate (80:20 v/v)

出典と根拠

ORDレコード
ord-5ff4dca0f4d145a982394eb6cbe6f53e
出典データセット
uspto-grants-2000_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06048864

反応ノート

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