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Hydroxylamine HCl → HCID 19971654、化合物

HRID 975255
ノート
印刷プレビュー

反応式

HRID 975255 の反応式
[CH3:1][O:2][CH2:3][CH2:4][CH2:5][CH2:6][C:7]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)=O.[Cl-].[OH:16][NH3+:17]>N1C=CC=CC=1>[CH3:1][O:2][CH2:3][CH2:4][CH2:5][CH2:6]/[C:7](/[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)=[N:17]/[OH:16]
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 21645Hydroxylamine HClHCID 119662825-Methoxy-1-phenyl-1-pentanone

生成物 1

HCID 19971654HCID 19971654、化合物収率 76%

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

実験手順

A mixture of the above ketone (8.8 g, 46 mmol), hydroxylammonium chloride (5.5 g, 78 mmol) and anhydrous pyridine (50 ml) was heated at reflux for 16 h. The reaction mixture was allowed to cool to room temperature and the solvent then evaporated in vacuo. To the residue was added 10% aqueous citric acid (100 ml) and the mixture was extracted with ethyl acetate (100 ml+50 ml). The combined organic phases were washed with 10% aqueous citric acid (25 ml), brine (25 ml) and dried (Na2SO4). The solvent was evaporated in vacuo and the residue purified by column chromatography on silica gel (250 g, n-heptane/ethyl acetate gradient 1/4 to 1/2 to give 7.25 g of Z-5-methoxy-1-phenyl-1-pentanone oxime as a colourless oil.

後処理

  1. temperaturewas heated
  2. temperatureat reflux for 16 h
  3. customthe solvent then evaporated in vacuo
  4. additionTo the residue was added 10% aqueous citric acid (100 ml)
  5. extractionthe mixture was extracted with ethyl acetate (100 ml+50 ml)
  6. washThe combined organic phases were washed with 10% aqueous citric acid (25 ml), brine (25 ml)
  7. dry with materialdried (Na2SO4)
  8. customThe solvent was evaporated in vacuo
  9. customthe residue purified by column chromatography on silica gel (250 g, n-heptane/ethyl acetate

出典と根拠

ORDレコード
ord-ab57a15f163d45439dbdab8fb1e68f07
出典データセット
uspto-grants-1997_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05608069

反応ノート

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