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Triethylamine → 1-(2,4,6-Trichlorophenyl)-2-propanone O-methyloxime

HRID 2381257
ノート
印刷プレビュー

反応式

HRID 2381257 の反応式
Cl.[CH3:2][O:3][NH2:4].C(N(CC)CC)C.[Cl:12][C:13]1[CH:18]=[C:17]([Cl:19])[CH:16]=[C:15]([Cl:20])[C:14]=1[CH2:21][C:22](=O)[CH3:23]>CO>[CH3:2][O:3][N:4]=[C:22]([CH3:23])[CH2:21][C:14]1[C:15]([Cl:20])=[CH:16][C:17]([Cl:19])=[CH:18][C:13]=1[Cl:12]
参加物反応条件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 8471TriethylamineHCID 521874O-Methylhydroxylamine hydrochlorideHCID 584436631-(2,4,6-Trichlorophenyl)-2-propanone

生成物 1

HCID 767875151-(2,4,6-Trichlorophenyl)-2-propanone O-methyloxime収率 76%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
60 °C

実験手順

A solution of O-methyl-hydroxylamine hydrochloride (0.79 g, 9.4 mmol) in methanol (20 ml) was treated with triethylamine (1.32 ml, 9.4 mmol) followed by 1-(2,4,6-trichlorophenyl)-propan-2-one (1.5 g, 6.31 mmole). The resulting mixture was stirred at 60° C. for 3 hours. The reaction mixture was quenched with water and methanol was evaporated off. The resulting aqueous medium was extracted with ethylacetate (3×50 ml). The combined organic layers were washed with brine and dried over anhydrous Na2SO4. The solvent was evaporated under reduced pressure (100 mbar; 45° C.). The resulting crude mass was purified by column chromatography using 60-120μ mesh silica gel and product collected at 2% ethyl acetate in hexane as elution system to give 1-(2,4,6-Trichloro-phenyl)-propan-2-one O-methyl-oxime (1.2 g, 76%), which was taken up for further reduction.

後処理

  1. customThe reaction mixture was quenched with water and methanol
  2. customwas evaporated off
  3. extractionThe resulting aqueous medium was extracted with ethylacetate (3×50 ml)
  4. washThe combined organic layers were washed with brine
  5. dry with materialdried over anhydrous Na2SO4
  6. customThe solvent was evaporated under reduced pressure (100 mbar; 45° C.)
  7. customThe resulting crude mass was purified by column chromatography
  8. customcollected at 2% ethyl acetate in hexane as elution system

出典と根拠

ORDレコード
ord-fdfa6c25699b4fa8a85eb7bd18158c55
出典データセット
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08258169B2

反応ノート

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